Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature
Author(s) -
Richard H. van Jaarsveld,
Jack Reilly,
Marie-Claire Cornips,
Michael A. Hadders,
Emanuele Agolini,
Priyanka Ahimaz,
Kwame AnyaneYeboa,
Séverine Audebert Bellanger,
Ellen van Binsbergen,
Marie-José van den Boogaard,
Elise BrischouxBoucher,
Raymond C. Caylor,
Andrea Ciolfi,
Ton A.J. van Essen,
Paolo Fontana,
Saskia Hopman,
Maria Iascone,
Margaret M. Javier,
ErikJan Kamsteeg,
Jennifer Kerkhof,
Jun Kido,
HyungGoo Kim,
Tjitske Kleefstra,
Fortunato Lonardo,
Abbe Lai,
Dorit Lev,
Michael A. Levy,
M. E. Suzanne Lewis,
Angie Lichty,
Marcel M.A.M. Mannens,
Naomichi Matsumoto,
Idit Maya,
Haley McConkey,
André Mégarbané,
Vincent Michaud,
Evelina Miele,
Marcello Niceta,
Antonio Novelli,
Roberta Onesimo,
Rolph Pfundt,
Bernt Popp,
Eloise J. Prijoles,
Raissa Relator,
Sylvia Redon,
Dmitrijs Rots,
Karen Rouault,
Ken Saida,
Jolanda Schieving,
Marco Tartaglia,
Romano Tenconi,
Kévin Uguen,
Nienke E. Verbeek,
Christopher A. Walsh,
Keren Yosovich,
Christopher J. Yuskaitis,
Giuseppe Zampino,
Bekim Sadiković,
Mariëlle Alders,
Renske Oegema
Publication year - 2022
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1016/j.gim.2022.09.006
Subject(s) - epigenetics , genetics , autism , biology , dna methylation , missense mutation , phenotype , psychiatry , medicine , gene , gene expression
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