Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression.

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Human Genetics, Vol. 111, Iss. 2, 2002-08 ,pp. : 190-197

Springer Publishing Company

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In vitro and in vivo suppression of GJB2 expression by RNA interference

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Did the GJB2 35delG mutation originate in Iran?

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American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2453-2458

John Wiley & Sons Inc

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

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

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

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