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Q36559231-48A9591E-B625-45B8-8607-490310D8344C
Q36559231-48A9591E-B625-45B8-8607-490310D8344C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36559231-48A9591E-B625-45B8-8607-490310D8344C
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
P2860
Q36559231-48A9591E-B625-45B8-8607-490310D8344C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36559231-48A9591E-B625-45B8-8607-490310D8344C
rank
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type
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Statement
wasDerivedFrom
5cad5c2eff1937e0772fa7c67abb0cd56ff51260
P2860
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling