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

By Meşe Gülistan   Londin Eric   Mui Rickie   Brink Peter   White Thomas  

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

Springer Publishing Company

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

Oxford University Press

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A Gene for Non-Syndromic Autosomal Dominant Progressive Postlingual Sensorineural Hearing Loss Maps to Chromosome 14q12–13

By Manolis Evangelos N.  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1047-1050

Oxford University Press

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A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10 , Maps to Chromosome 6

By O'Neill Marsha E.   Marietta Jacquie   Nishimura Darryl   Wayne Sigrid   Van Camp Guy   Van Laer Lut   Negrini Clelia   Wilcox Edward R.   Chen Achih   Fukushima Kunihiro   Ni Li   Sheffield Val C.   Smith Richard J. H.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 853-856

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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