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Q41311819-0140DF08-7E2A-42B3-99B6-DE02102FEC54
Q41311819-0140DF08-7E2A-42B3-99B6-DE02102FEC54
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41311819-0140DF08-7E2A-42B3-99B6-DE02102FEC54
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss.
P2860
Q41311819-0140DF08-7E2A-42B3-99B6-DE02102FEC54
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41311819-0140DF08-7E2A-42B3-99B6-DE02102FEC54
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
f1391d6cc981f578341ec297315c1448310a9a9c
P2860
Short Report - Clinical Genetics Genomic copy number alterations in non-syndromic hearing loss.