Open AccessCorrespondence on “Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype” by Zanoni et al
Author(s) -
Anna M. CuetoGonzález,
Paula FernándezÁlvarez,
Irene Valenzuela,
Amaia LasaAranzasti,
Teresa Vendrell Bayona,
Eduardo F. Tizzano
Publication year - 2021
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.2021.11.007
Subject(s) - microcephaly , missense mutation , intellectual disability , genetics , phenotype , hypotonia , craniofacial , loss function , developmental disorder , global developmental delay , autism , biology , gene , psychology , developmental psychology
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