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Q30476608-259ABB21-6DA3-465C-ADB2-C92A9FA1799B
Q30476608-259ABB21-6DA3-465C-ADB2-C92A9FA1799B
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http://www.wikidata.org/entity/statement/Q30476608-259ABB21-6DA3-465C-ADB2-C92A9FA1799B
Deafness and retinal degeneration in a novel USH1C knock-in mouse model
P2860
Q30476608-259ABB21-6DA3-465C-ADB2-C92A9FA1799B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30476608-259ABB21-6DA3-465C-ADB2-C92A9FA1799B
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wasDerivedFrom
22cf93d05337179c1f9e6e1ff800c537cbd60552
P2860
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin