TY  - GEN
AU  - Bouhouche,Ahmed
AU  - Birouk,Nazha
AU  - Azzedine,Hamid
AU  - Benomar,Ali
AU  - Durosier,Garry
AU  - Ente,Dorothée
AU  - Muriel,Marie-Paule
AU  - Ruberg,Merle
AU  - Slassi,Ilham
AU  - Yahyaoui,Mohamed
AU  - Dubourg,Odile
AU  - Ouazzani,Reda
AU  - LeGuern,Eric
TI  - Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families
SN  - 1460-2156
PY  - 2007///0530
KW  - Action Potentials
KW  - physiology
KW  - Adolescent
KW  - Adult
KW  - Axons
KW  - Charcot-Marie-Tooth Disease
KW  - ethnology
KW  - Child
KW  - Child, Preschool
KW  - Consanguinity
KW  - Electromyography
KW  - Female
KW  - Founder Effect
KW  - Genes, Dominant
KW  - genetics
KW  - Genotype
KW  - Humans
KW  - Lamin Type A
KW  - Lod Score
KW  - Male
KW  - Morocco
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Neural Conduction
KW  - Pedigree
KW  - Peroneal Nerve
KW  - pathology
KW  - Phenotype
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/brain/awm014
ER  -