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Q48718643-C2647DE0-66F3-41F2-A6EB-F4AB079B401F
Q48718643-C2647DE0-66F3-41F2-A6EB-F4AB079B401F
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http://www.wikidata.org/entity/statement/Q48718643-C2647DE0-66F3-41F2-A6EB-F4AB079B401F
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
P2860
Q48718643-C2647DE0-66F3-41F2-A6EB-F4AB079B401F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48718643-C2647DE0-66F3-41F2-A6EB-F4AB079B401F
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5dbeb972c0183491eb80f441e89d6d28b88b46da
P2860
Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing.