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Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
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