Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025))

Elisabeth M. Lodder; Pasquelena De Nittis; Charlotte D. Koopman; Wojciech Wiszniewski; Carolina Fischinger Moura de Souza; Najim Lahrouchi; Nicolas Guex; Valerio Napolioni; Federico Tessadori; Leander Beekman; Eline A. Nannenberg; Lamiae Boualla; Nico A. Blom; Wim de Graaff; Maarten Kamermans; Dario Cocciadiferro; Natascia Malerba; Barbara Mandriani; Zeynep Hande Coban Akdemir; Richard J. Fish; Mohammad K. Eldomery; Ilham Ratbi; Arthur A.M. Wilde; Teun de Boer; William F. Simonds; Marguerite Neerman-Arbez; V. Reid Sutton; Fernando Kok; James R. Lupski; Alexandre Reymond; Connie R. Bezzina; Jeroen Bakkers; Giuseppe Merla

doi:https://doi.org/10.1016/j.ajhg.2016.08.011

Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025))

Elisabeth M. Lodder, Pasquelena De Nittis, Charlotte D. Koopman, Wojciech Wiszniewski, Carolina Fischinger Moura de Souza, Najim Lahrouchi, Nicolas Guex, Valerio Napolioni, Federico Tessadori, Leander Beekman, Eline A. Nannenberg, Lamiae Boualla, Nico A. Blom, Wim de Graaff, Maarten Kamermans, Dario Cocciadiferro, Natascia Malerba, Barbara Mandriani, Zeynep Hande Coban Akdemir, Richard J. FishMohammad K. Eldomery, Ilham Ratbi, Arthur A.M. Wilde, Teun de Boer, William F. Simonds, Marguerite Neerman-Arbez, V. Reid Sutton, Fernando Kok, James R. Lupski, Alexandre Reymond, Connie R. Bezzina, Jeroen Bakkers, Giuseppe Merla

Research output: Contribution to journal › Comment/Letter to the editor › Academic

11 Citations (Scopus)

Abstract

(The American Journal of Human Genetics 99, 704–710; September 1, 2016) In the originally published version of this paper, several cells in Table 1 were incorrect. “Lexical production” has now been revised from “nonverbal” to “delayed” for both individuals in family E, and “light RV dilatation” has now been deleted from the “Heart structural abnormalities” row for individual II.1 in family E. Additionally, all instances of “NR” and “NT” (for “not reported” and “not tested”) have been revised to “NA” (for “not available”) throughout. The table is now correct both online and in print. The authors regret these errors and any confusion that might have resulted. Finally, due to technical error, the Supplemental Data file was not complete in the originally published version but now includes all relevant supplemental figures and tables.

Original language	English
Pages (from-to)	786
Number of pages	1
Journal	American journal of human genetics
Volume	99
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2016.08.011
Publication status	Published - 1 Sept 2016

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Lodder, E. M., De Nittis, P., Koopman, C. D., Wiszniewski, W., Moura de Souza, C. F., Lahrouchi, N., Guex, N., Napolioni, V., Tessadori, F., Beekman, L., Nannenberg, E. A., Boualla, L., Blom, N. A., de Graaff, W., Kamermans, M., Cocciadiferro, D., Malerba, N., Mandriani, B., Coban Akdemir, Z. H., ... Merla, G. (2016). Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025)). American journal of human genetics, 99(3), 786. https://doi.org/10.1016/j.ajhg.2016.08.011

Lodder, Elisabeth M. ; De Nittis, Pasquelena ; Koopman, Charlotte D. et al. / Erratum : GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025)). In: American journal of human genetics. 2016 ; Vol. 99, No. 3. pp. 786.

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title = "Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025))",

abstract = "(The American Journal of Human Genetics 99, 704–710; September 1, 2016) In the originally published version of this paper, several cells in Table 1 were incorrect. “Lexical production” has now been revised from “nonverbal” to “delayed” for both individuals in family E, and “light RV dilatation” has now been deleted from the “Heart structural abnormalities” row for individual II.1 in family E. Additionally, all instances of “NR” and “NT” (for “not reported” and “not tested”) have been revised to “NA” (for “not available”) throughout. The table is now correct both online and in print. The authors regret these errors and any confusion that might have resulted. Finally, due to technical error, the Supplemental Data file was not complete in the originally published version but now includes all relevant supplemental figures and tables.",

author = "Lodder, {Elisabeth M.} and {De Nittis}, Pasquelena and Koopman, {Charlotte D.} and Wojciech Wiszniewski and {Moura de Souza}, {Carolina Fischinger} and Najim Lahrouchi and Nicolas Guex and Valerio Napolioni and Federico Tessadori and Leander Beekman and Nannenberg, {Eline A.} and Lamiae Boualla and Blom, {Nico A.} and {de Graaff}, Wim and Maarten Kamermans and Dario Cocciadiferro and Natascia Malerba and Barbara Mandriani and {Coban Akdemir}, {Zeynep Hande} and Fish, {Richard J.} and Eldomery, {Mohammad K.} and Ilham Ratbi and Wilde, {Arthur A.M.} and {de Boer}, Teun and Simonds, {William F.} and Marguerite Neerman-Arbez and Sutton, {V. Reid} and Fernando Kok and Lupski, {James R.} and Alexandre Reymond and Bezzina, {Connie R.} and Jeroen Bakkers and Giuseppe Merla",

note = "Publisher Copyright: {\textcopyright} 2016 American Society of Human Genetics",

year = "2016",

month = sep,

day = "1",

doi = "https://doi.org/10.1016/j.ajhg.2016.08.011",

language = "English",

volume = "99",

pages = "786",

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Lodder, EM, De Nittis, P, Koopman, CD, Wiszniewski, W, Moura de Souza, CF, Lahrouchi, N, Guex, N, Napolioni, V, Tessadori, F, Beekman, L , Nannenberg, EA, Boualla, L, Blom, NA, de Graaff, W, Kamermans, M, Cocciadiferro, D, Malerba, N, Mandriani, B, Coban Akdemir, ZH, Fish, RJ, Eldomery, MK, Ratbi, I, Wilde, AAM, de Boer, T, Simonds, WF, Neerman-Arbez, M, Sutton, VR, Kok, F, Lupski, JR, Reymond, A, Bezzina, CR, Bakkers, J & Merla, G 2016, 'Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025))', American journal of human genetics, vol. 99, no. 3, pp. 786. https://doi.org/10.1016/j.ajhg.2016.08.011

Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025)). / Lodder, Elisabeth M.; De Nittis, Pasquelena; Koopman, Charlotte D. et al.
In: American journal of human genetics, Vol. 99, No. 3, 01.09.2016, p. 786.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Erratum

T2 - GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025))

AU - Lodder, Elisabeth M.

AU - De Nittis, Pasquelena

AU - Koopman, Charlotte D.

AU - Wiszniewski, Wojciech

AU - Moura de Souza, Carolina Fischinger

AU - Lahrouchi, Najim

AU - Guex, Nicolas

AU - Napolioni, Valerio

AU - Tessadori, Federico

AU - Beekman, Leander

AU - Nannenberg, Eline A.

AU - Boualla, Lamiae

AU - Blom, Nico A.

AU - de Graaff, Wim

AU - Kamermans, Maarten

AU - Cocciadiferro, Dario

AU - Malerba, Natascia

AU - Mandriani, Barbara

AU - Coban Akdemir, Zeynep Hande

AU - Fish, Richard J.

AU - Eldomery, Mohammad K.

AU - Ratbi, Ilham

AU - Wilde, Arthur A.M.

AU - de Boer, Teun

AU - Simonds, William F.

AU - Neerman-Arbez, Marguerite

AU - Sutton, V. Reid

AU - Kok, Fernando

AU - Lupski, James R.

AU - Reymond, Alexandre

AU - Bezzina, Connie R.

AU - Bakkers, Jeroen

AU - Merla, Giuseppe

PY - 2016/9/1

Y1 - 2016/9/1

N2 - (The American Journal of Human Genetics 99, 704–710; September 1, 2016) In the originally published version of this paper, several cells in Table 1 were incorrect. “Lexical production” has now been revised from “nonverbal” to “delayed” for both individuals in family E, and “light RV dilatation” has now been deleted from the “Heart structural abnormalities” row for individual II.1 in family E. Additionally, all instances of “NR” and “NT” (for “not reported” and “not tested”) have been revised to “NA” (for “not available”) throughout. The table is now correct both online and in print. The authors regret these errors and any confusion that might have resulted. Finally, due to technical error, the Supplemental Data file was not complete in the originally published version but now includes all relevant supplemental figures and tables.

AB - (The American Journal of Human Genetics 99, 704–710; September 1, 2016) In the originally published version of this paper, several cells in Table 1 were incorrect. “Lexical production” has now been revised from “nonverbal” to “delayed” for both individuals in family E, and “light RV dilatation” has now been deleted from the “Heart structural abnormalities” row for individual II.1 in family E. Additionally, all instances of “NR” and “NT” (for “not reported” and “not tested”) have been revised to “NA” (for “not available”) throughout. The table is now correct both online and in print. The authors regret these errors and any confusion that might have resulted. Finally, due to technical error, the Supplemental Data file was not complete in the originally published version but now includes all relevant supplemental figures and tables.

UR - http://www.scopus.com/inward/record.url?scp=85020538072&partnerID=8YFLogxK

U2 - https://doi.org/10.1016/j.ajhg.2016.08.011

DO - https://doi.org/10.1016/j.ajhg.2016.08.011

M3 - Comment/Letter to the editor

SN - 0002-9297

VL - 99

SP - 786

JO - American journal of human genetics

JF - American journal of human genetics

IS - 3

ER -

Lodder EM, De Nittis P, Koopman CD, Wiszniewski W, Moura de Souza CF, Lahrouchi N et al. Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025)). American journal of human genetics. 2016 Sept 1;99(3):786. doi: https://doi.org/10.1016/j.ajhg.2016.08.011

Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025))

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