Connexin32 in the peripheral nervous system. Functional analysis of mutations associated with X-linked Charcot-Marie-Tooth syndrome and implications for the pathophysiology of the disease.

Authors :: Nicholson SM
Ressot C
Gomès D
D'Andrea P
Perea J
Duval N
Bruzzone R
Source :: Annals of the New York Academy of Sciences [Ann N Y Acad Sci] 1999 Sep 14; Vol. 883, pp. 168-85.
Publication Year :: 1999

Subjects :: Animals
Connexins chemistry
Connexins physiology
Humans
Protein Conformation
X Chromosome
Gap Junction beta-1 Protein
Charcot-Marie-Tooth Disease genetics
Charcot-Marie-Tooth Disease physiopathology
Connexins genetics
Mutation

Tools