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Q41311819-5142C3A2-EAA4-4BCE-8CB8-6293F141AA9F
Q41311819-5142C3A2-EAA4-4BCE-8CB8-6293F141AA9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41311819-5142C3A2-EAA4-4BCE-8CB8-6293F141AA9F
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss.
P2860
Q41311819-5142C3A2-EAA4-4BCE-8CB8-6293F141AA9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41311819-5142C3A2-EAA4-4BCE-8CB8-6293F141AA9F
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type
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Statement
wasDerivedFrom
f1391d6cc981f578341ec297315c1448310a9a9c
P2860
Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.