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Q40542422-C89659E1-80AE-4977-93FF-AFD50A114466
Q40542422-C89659E1-80AE-4977-93FF-AFD50A114466
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http://www.wikidata.org/entity/statement/Q40542422-C89659E1-80AE-4977-93FF-AFD50A114466
Transport and function of cx26 mutants involved in skin and deafness disorders.
P2860
Q40542422-C89659E1-80AE-4977-93FF-AFD50A114466
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40542422-C89659E1-80AE-4977-93FF-AFD50A114466
rank
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wasDerivedFrom
077d7ea20c8a19761dd23b121eb66a9bd35582e2
P2860
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families.