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Q48718643-A91B7164-46AE-4B8B-BE83-8C24115873AA
Q48718643-A91B7164-46AE-4B8B-BE83-8C24115873AA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48718643-A91B7164-46AE-4B8B-BE83-8C24115873AA
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
P2860
Q48718643-A91B7164-46AE-4B8B-BE83-8C24115873AA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48718643-A91B7164-46AE-4B8B-BE83-8C24115873AA
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
5dbeb972c0183491eb80f441e89d6d28b88b46da
P2860
A mutation in PDS causes non-syndromic recessive deafness