Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

David P. Kelsell, John Dunlop, Howard P. Stevens et al. · Nature · 1997 · 1.5K citations

Life Sciences, Genetics, Molecular Genetics +13

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 636 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

Leopoldo Zelante · Human Molecular Genetics · 1997 · 627 citations

Life Sciences, Genetics, Molecular Genetics +16

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

Gabriele Richard, Lisa E. Smith, Regina A. Bailey et al. · Nature Genetics · 1998 · 345 citations

Life Sciences, Genetics, Molecular Genetics +3

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

David Robinson · Journal of Medical Genetics · 1999 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12