Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination

Author:

Warner Laura E,Hilz Max J,Appel Stanley H,Killian James M,Kolodny Edwin H,Karpati George,Carpenter Stirling,Watters Gordon V,Wheeler Calvin,Witt David,Bodell Adria,Nelis Eva,Van Broeckhoven Christine,Lupski James R

Publisher

Elsevier BV

Subject

General Neuroscience

Reference54 articles.

1. Infantile hereditary neuropathy with hypomyelination;Balestrini;Neuropediatrics,1991

2. Identification of a 4 bp deletion (1560del4) in P0 gene in a family with severe Charcot–Marie–Tooth disease;Bellone;Hum. Mut,1996

3. Evidence for linkage of Charcot–Marie–Tooth neuropathy to the Duffy locus on chromosome 1;Bird;Am. J. Hum. Genet,1982

4. Charcot–Marie–Tooth type 1B neuropathy;Blanquet-Grossard;Clin. Genet,1995

5. Charcot–Marie–Tooth type 1B;Blanquet-Grossard;Hum. Mut., in press,1996

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