Identical point mutations of PMP–22 in Trembler–J mouse and Charcot–Marie–Tooth disease type 1A

Author:

Valentijn Linda J.,Baas Frank,Wolterman Ruud A.,Hoogendijk Jessica E.,van den Bosch Norbert H.A.,Zorn Ina,Gabreëls-Festen Anneke A.W.M.,de Visser Marianne,Bolhuis Pieter A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference31 articles.

1. Harding, A.E. & Thomas, P.K. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain 103, 259–280 (1980).

2. Hoogendijk, J.E. & De Visser, M. in Handbook of Clinical Neurology. Hereditary neuropathies and spinocerebellar atrophies. Vol. 60 (eds Vinken, P.J. et al.).(Elsevier, Amsterdam, 1991).

3. Vance, J.M. et al. Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17. Exp. Neurology. 104, 186–189 (1989).

4. Vance, J.M. et al. Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2. Genomics 9, 623–628 (1991).

5. 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).

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