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Human Molecular Genetics, Vol. 6, Iss. 12, 1997-11 ,pp. : 2173-2177

Oxford University Press

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Progress in Understanding GJB2-Linked Deafness

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Mutation Analysis of a Mauritian Hereditary Breast Cancer Family Reveals the BRCA2 6503delTT Mutation Previously Found to Recur in Different Ethnic Populations

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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

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

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