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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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Comment on Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3
1Department of Laboratories, Seattle Children's Hospital, Seattle, WA, USA. madelyn.gillentine@seattlechildrens.org.
European Journal of Human Genetics : EJHG
|November 28, 2023
Abstract
No abstract available in PubMed .
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