TY - JOUR
T1 - Erratum: LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance (Brain (2016) 139 (782-794) DOI: 10.1093/brain/awv392)
AU - Dallabona, Cristina
AU - Abbink, Truus E. M.
AU - Carrozzo, Rosalba
AU - Torraco, Alessandra
AU - Legati, Andrea
AU - van Berkel, Carola G. M.
AU - Niceta, Marcello
AU - Langella, Tiziana
AU - Verrigni, Daniela
AU - Rizza, Teresa
AU - Diodato, Daria
AU - Piemonte, Fiorella
AU - Lamantea, Eleonora
AU - Fang, Mingyan
AU - Zhang, Jianguo
AU - Martinelli, Diego
AU - Bevivino, Elsa
AU - Dionisi-Vici, Carlo
AU - Vanderver, Adeline
AU - Philip, Sunny G.
AU - Kurian, Manju A.
AU - Verma, Ishwar C.
AU - Bijarnia-Mahay, Sunita
AU - Jacinto, Sandra
AU - Furtado, Fatima
AU - Accorsi, Patrizia
AU - Ardissone, Anna
AU - Moroni, Isabella
AU - Ferrero, Ileana
AU - Tartaglia, Marco
AU - Goffrini, Paola
AU - Ghezzi, Daniele
AU - van der Knaap, Marjo S.
AU - Bertini, Enrico
PY - 2018
Y1 - 2018
N2 - Cristina Dallabona, Truus E. M. Abbink, Rosalba Carrozzo, Alessandra Torraco, Andrea Legati, Carola G. M. van Berkel, Marcello Niceta, Tiziana Langella, Daniela Verrigni, Teresa Rizza, Daria Diodato, Fiorella Piemonte, Eleonora Lamantea, Mingyan Fang, Jianguo Zhang, Diego Martinelli, Elsa Bevivino, Carlo Dionisi-Vici, Adeline Vanderver, Sunny G. Philip, Manju A. Kurian, Ishwar C. Verma, Sunita Bijarnia-Mahay, Sandra Jacinto, Fatima Furtado, Patrizia Accorsi, Anna Ardissone, Isabella Moroni, Ileana Ferrero, Marco Tartaglia, Paola Goffrini, Daniele Ghezzi, Marjo S. van der Knaap and Enrico Bertini. LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance. Brain 2016; 139: 782-794. doi:10.1093/brain/awv392. The authors apologize for mixing the mutations of Patients 5 and 7 on pages 788 and 789 in Figure 2 and its legend, in the main text and the online Supplementary Tables. This has now been corrected online. On page 788, the text should read: Sanger sequencing of the entire coding sequence of LYRM7 and intron-exon boundaries was performed in three additional patients. Patient 5 was found homozygous for the c.37delA (p.Thr13Hisfs∗17) mutation, which is predicted to dramatically affect recognition of the splice donor motif of exon 4 and likely impair proper RNA splicing (Fig. 2M and N), while Patients 6 and 7 were found to be homozygous for the c.214C4T (p.Q72∗) (Fig. 2L), and c.243-244 + 2delGAGT (p.?) (Fig. 2H) mutations, respectively. The Supplementary Tables have been corrected online. On page 789, Figure 2 and legend should be as follows.
AB - Cristina Dallabona, Truus E. M. Abbink, Rosalba Carrozzo, Alessandra Torraco, Andrea Legati, Carola G. M. van Berkel, Marcello Niceta, Tiziana Langella, Daniela Verrigni, Teresa Rizza, Daria Diodato, Fiorella Piemonte, Eleonora Lamantea, Mingyan Fang, Jianguo Zhang, Diego Martinelli, Elsa Bevivino, Carlo Dionisi-Vici, Adeline Vanderver, Sunny G. Philip, Manju A. Kurian, Ishwar C. Verma, Sunita Bijarnia-Mahay, Sandra Jacinto, Fatima Furtado, Patrizia Accorsi, Anna Ardissone, Isabella Moroni, Ileana Ferrero, Marco Tartaglia, Paola Goffrini, Daniele Ghezzi, Marjo S. van der Knaap and Enrico Bertini. LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance. Brain 2016; 139: 782-794. doi:10.1093/brain/awv392. The authors apologize for mixing the mutations of Patients 5 and 7 on pages 788 and 789 in Figure 2 and its legend, in the main text and the online Supplementary Tables. This has now been corrected online. On page 788, the text should read: Sanger sequencing of the entire coding sequence of LYRM7 and intron-exon boundaries was performed in three additional patients. Patient 5 was found homozygous for the c.37delA (p.Thr13Hisfs∗17) mutation, which is predicted to dramatically affect recognition of the splice donor motif of exon 4 and likely impair proper RNA splicing (Fig. 2M and N), while Patients 6 and 7 were found to be homozygous for the c.214C4T (p.Q72∗) (Fig. 2L), and c.243-244 + 2delGAGT (p.?) (Fig. 2H) mutations, respectively. The Supplementary Tables have been corrected online. On page 789, Figure 2 and legend should be as follows.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85057276594&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/30137257
U2 - https://doi.org/10.1093/brain/awy194
DO - https://doi.org/10.1093/brain/awy194
M3 - Erratum/Corrigendum
C2 - 30137257
SN - 0006-8950
VL - 141
SP - e82
JO - Brain
JF - Brain
IS - 11
ER -