Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families. [electronic resource]
Producer: 20070530Description: 1062-75 p. digitalISSN:- 1460-2156
- Action Potentials -- physiology
- Adolescent
- Adult
- Axons -- physiology
- Charcot-Marie-Tooth Disease -- ethnology
- Child
- Child, Preschool
- Consanguinity
- Electromyography
- Female
- Founder Effect
- Genes, Dominant -- genetics
- Genotype
- Humans
- Lamin Type A -- genetics
- Lod Score
- Male
- Morocco
- Mutation -- genetics
- Nerve Tissue Proteins -- genetics
- Neural Conduction -- physiology
- Pedigree
- Peroneal Nerve -- pathology
- Phenotype
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.