Bouhouche, Ahmed <br/><br/>
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.  [electronic resource] 

 -  Brain : a journal of neurology  Apr 2007 
 - 1062-75 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awm014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Action Potentials--physiology<br/>Adolescent<br/>Adult<br/>Axons--physiology<br/>Charcot-Marie-Tooth Disease--ethnology<br/>Child<br/>Child, Preschool<br/>Consanguinity<br/>Electromyography<br/>Female<br/>Founder Effect<br/>Genes, Dominant--genetics<br/>Genotype<br/>Humans<br/>Lamin Type A--genetics<br/>Lod Score<br/>Male<br/>Morocco<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>Neural Conduction--physiology<br/>Pedigree<br/>Peroneal Nerve--pathology<br/>Phenotype