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RSK2 mutation co‐segregates with X‐linked intellectual disability and attenuated Coffin–Lowry phenotype in a three‐generation family
Author(s) -
Maystadt I,
Destree A,
Benoit V,
Aeby A,
Lederer D,
Moortgat S,
Jurkiewicz D,
KrajewskaWalasek M,
Hanauer A,
Thomas GM
Publication year - 2014
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12122
Subject(s) - medical genetics , medicine , genetics , library science , gerontology , biology , gene , computer science
SCOPUS: le.jFLWINinfo:eu-repo/semantics/publishe
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