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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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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Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

By Aoki Y.  

Human Molecular Genetics, Vol. 12, Iss. 9, 2003-05 ,pp. : 995-1004

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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Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan

By Veske Andres   Oehlmann Ralph   Younus Farah   Mohyuddin Aisha   Müller-Myhsok Bertram   Qasim Mehdi S.   Gal Andreas  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 165-168

Oxford University Press

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