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Q48718643-04077121-FD7A-426D-B7D8-1380A31E468E
Q48718643-04077121-FD7A-426D-B7D8-1380A31E468E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48718643-04077121-FD7A-426D-B7D8-1380A31E468E
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
P2860
Q48718643-04077121-FD7A-426D-B7D8-1380A31E468E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48718643-04077121-FD7A-426D-B7D8-1380A31E468E
rank
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Statement
wasDerivedFrom
5dbeb972c0183491eb80f441e89d6d28b88b46da
P2860
Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome.