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Q48718643-A9773E83-7F66-4AB2-B4B5-3445E3632B27
Q48718643-A9773E83-7F66-4AB2-B4B5-3445E3632B27
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48718643-A9773E83-7F66-4AB2-B4B5-3445E3632B27
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
P2860
Q48718643-A9773E83-7F66-4AB2-B4B5-3445E3632B27
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48718643-A9773E83-7F66-4AB2-B4B5-3445E3632B27
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Statement
wasDerivedFrom
5dbeb972c0183491eb80f441e89d6d28b88b46da
P2860
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)