Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness

By Balkany T.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2945-2951

Oxford University Press

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Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

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Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1605-1609

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Novel mutations in the connexin43 () and pseudogene may contribute to nonsyndromic hearing loss

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Human Genetics, Vol. 127, Iss. 5, 2010-05 ,pp. : 545-551

Springer Publishing Company

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Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss

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Human Genetics, Vol. 115, Iss. 3, 2004-08 ,pp. : 191-199

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Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations

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