De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females
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Published:2021-04
Issue:4
Volume:23
Page:637-644
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Li Dong,
Strong Alanna,
Shen Kaitlyn M.,
Cassiman David,
Van Dyck Maria,
Linhares Natalia Duarte,
Valadares Eugenia Ribeiro,
Wang Tiancheng,
Pena Sergio D.J.,
Jaeken Jaak,
Vergano Samantha,
Zackai Elaine,
Hing Anne,
Chow Penny,
Ganguly Arupa,
Scholz Tasja,
Bierhals Tatjana,
Philipp Deindl,
Hakonarson Hakon,
Bhoj ElizabethORCID
Subject
Genetics (clinical)
Cited by
16 articles.
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