Mutations in GJA1(connexin43) are associated with non-syndromic autosomal recessive deafness.
Liu, Xue Zhong; Xia, XiaJuan; Adams, Joe; Chen, Zheng Yi; Welch, KatherineO.; Tekin, Mustafa; Ouyang, Xiao Mei; Kristiansen, Arther; Pandya, Arti; Balkany, Thomas; Arnos, Kathleen S.; Nance, Walter E.; Human Molecular Genetics, 2001, vol. 10, issue 25, p 2945, ISSN 09646906. ISBN 09646906.

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