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Nat Genet. 1993 Sep;5(1):31-4.

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene.

Author information

1
Department of Pediatrics, Akita University School of Medicine, Japan.

Abstract

P0, a major structural protein of peripheral myelin, is a homophilic adhesion molecule and maps to chromosome 1q22-q23, in the region of the locus for Charcot-Marie-Tooth neuropathy type 1B (CMT1B). We have investigated P0 as a candidate gene in two pedigrees with CMT1B and found point mutations which are completely linked with the disease (Z = 5.5, theta = 0). The mutations, glutamate substitution for lysine 96 or aspartate 90, are located in the extracellular domain, which plays a significant role in myelin membrane adhesion. Individuals with CMT1B are heterozygous for the normal allele and the mutant allele. Our results indicate that P0 is a gene responsible for CMT1B.

PMID:
7693129
DOI:
10.1038/ng0993-31
[Indexed for MEDLINE]

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