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Q50437931-614A22DA-D18C-4C3C-BEBD-6A9FDED01537
Q50437931-614A22DA-D18C-4C3C-BEBD-6A9FDED01537
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http://www.wikidata.org/entity/statement/Q50437931-614A22DA-D18C-4C3C-BEBD-6A9FDED01537
A large cohort study of GJB2 mutations in Japanese hearing loss patients.
P2860
Q50437931-614A22DA-D18C-4C3C-BEBD-6A9FDED01537
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50437931-614A22DA-D18C-4C3C-BEBD-6A9FDED01537
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d64ea5f4f643f18676f7bb0558c2f5778043bda1
P2860
Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.