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Q41311819-516EC5CE-5819-480C-B8C9-6263AA9ABA80
Q41311819-516EC5CE-5819-480C-B8C9-6263AA9ABA80
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41311819-516EC5CE-5819-480C-B8C9-6263AA9ABA80
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss.
P2860
Q41311819-516EC5CE-5819-480C-B8C9-6263AA9ABA80
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41311819-516EC5CE-5819-480C-B8C9-6263AA9ABA80
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type
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Statement
wasDerivedFrom
042aa8080b84802952cd9f4db1aef15ae506ee5c
P2860
Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.