[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan]. [electronic resource]
Producer: 20090122Description: 1385-91 p. digitalISSN:- 0016-6758
- Alleles
- Amino Acid Substitution
- Bashkiria -- ethnology
- Charcot-Marie-Tooth Disease -- diagnosis
- Connexins -- genetics
- Female
- Founder Effect
- Humans
- Linkage Disequilibrium
- Male
- Microsatellite Repeats -- genetics
- Mutation, Missense
- Polymorphism, Genetic
- Quantitative Trait Loci -- genetics
- Gap Junction beta-1 Protein
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Publication Type: English Abstract; Journal Article; Research Support, Non-U.S. Gov't
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