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

By Zelante Leopoldo   Gasparini Paolo   Estivill Xavier  

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

Oxford University Press

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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

By Carrasquillo Minerva M.   Zlotogora Joel   Barges Saleh   Chakravarti Aravinda  

Human Molecular Genetics, Vol. 6, Iss. 12, 1997-11 ,pp. : 2163-2172

Oxford University Press

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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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Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

By Liu Xue-Zhong  

Human Molecular Genetics, Vol. 9, Iss. 1, 2000-01 ,pp. : 63-67

Oxford University Press

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A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness ( DFNA11 ) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene

By Tamagawa Yuya   Kitamura Ken   Ishida Takashi   Ishikawa Kazuhiro   Tanaka Hajime   Tsuji Shoji   Nishizawa Masatoyo  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 849-852

Oxford University Press

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