Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. [electronic resource]
Producer: 20000302Description: 344-9 p. digitalISSN:- 0888-7543
- Charcot-Marie-Tooth Disease -- genetics
- Chromosome Mapping
- Chromosomes, Human, Pair 11 -- genetics
- Consanguinity
- Female
- Genes, Recessive
- Genetic Linkage
- Genetic Markers
- Genetic Testing
- Genotype
- Haplotypes
- Humans
- Lod Score
- Male
- Myelin Sheath -- genetics
- Neural Conduction -- genetics
- Pedigree
- Phenotype
- Protein Folding
- Tunisia
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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