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Q37637310-B8DE3904-B500-4718-925E-1B1D3636C634
Q37637310-B8DE3904-B500-4718-925E-1B1D3636C634
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37637310-B8DE3904-B500-4718-925E-1B1D3636C634
Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment.
P2860
Q37637310-B8DE3904-B500-4718-925E-1B1D3636C634
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37637310-B8DE3904-B500-4718-925E-1B1D3636C634
rank
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Statement
wasDerivedFrom
b5a8fc4f3c76f0dcaae335e911d9c88b1200b121
P2860
Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearing.