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

Author:

Hayasaka Kiyoshi,Himoro Masato,Sato Wataru,Takada Goro,Uyemura Keiichi,Shimizu Nobuyoshi,Bird Thomas D.,Conneally P. Michael,Chance Phillip F.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference33 articles.

1. Dyck, P.J., Chance, P., Lebo, R. & Carney, J.I. Hereditary motor and sensory neuropathies. in Peripheral neuropathy 3rd edn (eds Dyck, P.J. et al.) 1094–1136 (Saunders, Philadelphia, 1993).

2. Harding, A.E. & Thomas, P.K. Genetic aspects of hereditary motor and sensory neuropathy (type I and II). J. med. Genet. 17, 329–336 (1980).

3. Bird, T.D., Ott, J. & Giblett, E.R. Evidence for linkage of Charcot-Marie-Tooth disease to the duffy locus on chromosome 1. Am. J. hum. Genet. 34, 388–394 (1982).

4. Stebbins, N.B. & Conneally, P.M. Linkage of dominantly inherited Charcot-Marie-Tooth neuropathy to the duffy locus in an Indiana family (abstract). Am. J. hum. Genet. 34, 195A (1982).

5. Vance, J.M. et al. Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17. Exp. Neurol. 104, 186–189 (1989).

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