Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease

Ítems similars

• GJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot–Marie–Tooth disease
  per: Gonzaga-Jauregui, Claudia, et al.
  Publicat: (2010)
• Pathogenesis of X-Linked Charcot-Marie-Tooth Disease: Differential Effects of Two Mutations in Connexin 32
  per: Abrams, Charles K., et al.
  Publicat: (2003)
• Arginine-164-tryptophan substitution in connexin32 associated with X linked dominant Charcot-Marie-Tooth disease.
  per: Oterino, A, et al.
  Publicat: (1996)
• The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.
  per: Meggouh, F, et al.
  Publicat: (1998)
• Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease
  per: Braathen, Geir J, et al.
  Publicat: (2007)