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Q30476608-744B2F3E-A5E6-43C2-90A7-A704875DD89E
Q30476608-744B2F3E-A5E6-43C2-90A7-A704875DD89E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30476608-744B2F3E-A5E6-43C2-90A7-A704875DD89E
Deafness and retinal degeneration in a novel USH1C knock-in mouse model
P2860
Q30476608-744B2F3E-A5E6-43C2-90A7-A704875DD89E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30476608-744B2F3E-A5E6-43C2-90A7-A704875DD89E
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wasDerivedFrom
22cf93d05337179c1f9e6e1ff800c537cbd60552
P2860
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss