Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.
Liu XZ; Xia XJ; Adams J; Chen ZY; Welch KO; Tekin M; Ouyang XM; Kristiansen A; Pandya A; Balkany T; Arnos KS; Nance WE; Human Molecular Genetics, 2001, vol. 10, issue 25, p 2945, ISSN 09646906. ISBN 09646906.

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