Title: | La maladie de Charcot-Marie-Tooth |
Journal : | médecine/sciences (m/s), 26, 10 |
Authors: | Vallat JM ; Funalot B |
Material Type: | Article |
Publication Date: | 10/2010 |
Size: | p. 842-847 |
Languages: | French |
Keywords : | autosomal inheritance ; axonal transport ; Charcot-Marie-Tooth disease ; Charcot-Marie-Tooth disease, demyelinating, dominant autosomal (CMT1) ; CMT2 autosomal dominant form ; CMT2 autosomal recessive form ; connexin 32 ; diseases classifications ; EGR2 gene ; electron microscopy ; GDAP1 protein ; genetic mutations ; mitofusin ; MTMR2 gene ; muscle wasting ; myelin protein 22 ; myelin protein zero ; nerve biopsies ; nerve conduction velocity ; neurons ; peripheral nerves ; prevalence ; review article ; Schwann cells |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/20929675 |