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CNOT2 haploinsufficiency causes a neurodevelopmental disorder with characteristic facial features
Author(s) -
Uehara Tomoko,
Tsuchihashi Takatoshi,
Yamada Mamiko,
Suzuki Hisato,
Takenouchi Toshiki,
Kosaki Kenjiro
Publication year - 2019
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.61356
Subject(s) - haploinsufficiency , neurodevelopmental disorder , psychology , developmental psychology , cognitive psychology , genetics , biology , phenotype , autism , gene
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