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

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1997 • 1,435 citations

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

1997 • 635 citations

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

1997 • 613 citations

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

1998 • 343 citations

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

1999 • 29 citations

Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness

1998 • 21 citations

Hereditary palmoplantar keratoderma with deafness

1996 • 12 citations