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Q34811722-3BD0DA42-9D88-49B8-BEC6-9DC6576B2D3C
Q34811722-3BD0DA42-9D88-49B8-BEC6-9DC6576B2D3C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34811722-3BD0DA42-9D88-49B8-BEC6-9DC6576B2D3C
The large Chinese family with Y-linked hearing loss revisited: clinical investigation.
P2860
Q34811722-3BD0DA42-9D88-49B8-BEC6-9DC6576B2D3C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34811722-3BD0DA42-9D88-49B8-BEC6-9DC6576B2D3C
rank
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type
BestRank
Statement
wasDerivedFrom
ad6dbde494f10005b7ffd99b0149d9173a1294dd
P2860
A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.