A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein

By Gottfried I.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1311-1316

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 the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30

By Marziano N.K.  

Human Molecular Genetics, Vol. 12, Iss. 8, 2003-04 ,pp. : 805-812

Oxford University Press

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EKV mutant connexin 31 associated cell death is mediated by ER stress

By Tattersall Daniel   Scott Claire A.   Gray Colin   Zicha Daniel   Kelsell David P.  

Human Molecular Genetics, Vol. 18, Iss. 24, 2009-12 ,pp. : 4734-4745

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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