Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families

Ítems similars

• Genetic analysis of the connexin-26 M34T variant
  per: Griffith, A., et al.
  Publicat: (2001)
• A genotype-phenotype correlation for GJB2 (connexin 26) deafness
  per: Cryns, K, et al.
  Publicat: (2004)
• Connexin26 deafness in several interconnected families
  per: Wilcox, S., et al.
  Publicat: (1999)
• Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome
  per: Richard, Gabriele, et al.
  Publicat: (2002)
• Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss
  per: Houseman, M., et al.
  Publicat: (2001)