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2024-03-23T02:32:08Z
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Phenotypic expression of a Pro 87 to Leu mutation in the connexin 32 gene in a large Swiss family with Charcot-Marie-Tooth neuropathy
10.1016/S0022-510X(02)00394-5
12614935
000181533500013
T.
Kuntzer
author
M.
Dunand
author
D. F.
Schorderet
author
J. M.
Vallat
author
A. F.
Hahn
author
J.
Bogousslavsky
author
article
2003-03
Journal of the Neurological Sciences
0022-510X
journal
207
1-2
77-86
Adolescent Adult Aged Amino Acid Substitution/*genetics Charcot-Marie-Tooth Disease/*genetics/physiopathology Child Child, Preschool Connexins/*genetics Female Humans Leucine/*genetics Male Middle Aged Neural Conduction/genetics Pedigree Phenotype *Point Mutation Statistics, Nonparametric
Comparative Study Journal Article Research Support, Non-U.S. Gov't --- Old month value: Mar 15
60_published
peer-reviewed