Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

By Teubner Barbara  

Human Molecular Genetics, Vol. 12, Iss. 1, 2003-01 ,pp. : 13-21

Oxford University Press

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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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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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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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LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice

By Hartmann D.  

Human Molecular Genetics, Vol. 12, Iss. 6, 2003-03 ,pp. : 631-646

Oxford University Press

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