Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

Candy Kumps; Erika D’haenens; Jennifer Kerkhof; Haley McConkey; Marielle Alders; Bekim Sadikovic; Olivier M. Vanakker

doi:https://doi.org/10.1038/s41431-023-01459-w

Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

Candy Kumps, Erika D’haenens, Jennifer Kerkhof, Haley McConkey, Marielle Alders, Bekim Sadikovic, Olivier M. Vanakker

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

Original language	English
Pages (from-to)	1350-1354
Number of pages	5
Journal	European journal of human genetics
Volume	31
Issue number	12
Early online date	2023
DOIs	https://doi.org/10.1038/s41431-023-01459-w
Publication status	Published - Dec 2023

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https://doi.org/10.1038/s41431-023-01459-w

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title = "Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome",

author = "Candy Kumps and Erika D{\textquoteright}haenens and Jennifer Kerkhof and Haley McConkey and Marielle Alders and Bekim Sadikovic and Vanakker, {Olivier M.}",

note = "Funding Information: No funding or financial assistance was received in support of the study.",

year = "2023",

month = dec,

doi = "https://doi.org/10.1038/s41431-023-01459-w",

language = "English",

volume = "31",

pages = "1350--1354",

journal = "European journal of human genetics",

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Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome. / Kumps, Candy; D’haenens, Erika; Kerkhof, Jennifer et al.
In: European journal of human genetics, Vol. 31, No. 12, 12.2023, p. 1350-1354.

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

TY - JOUR

T1 - Methylation signatures in clinically variable syndromic disorders

T2 - a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

AU - Kumps, Candy

AU - D’haenens, Erika

AU - Kerkhof, Jennifer

AU - McConkey, Haley

AU - Alders, Marielle

AU - Sadikovic, Bekim

AU - Vanakker, Olivier M.

N1 - Funding Information: No funding or financial assistance was received in support of the study.

PY - 2023/12

Y1 - 2023/12

UR - http://www.scopus.com/inward/record.url?scp=85171787307&partnerID=8YFLogxK

U2 - https://doi.org/10.1038/s41431-023-01459-w

DO - https://doi.org/10.1038/s41431-023-01459-w

M3 - Comment/Letter to the editor

C2 - 37736838

SN - 1018-4813

VL - 31

SP - 1350

EP - 1354

JO - European journal of human genetics

JF - European journal of human genetics

IS - 12

ER -

Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

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