Heterozygous Null Mutation in the P0 Gene Associated with Mild Charcot‐Marie‐Tooth Disease
- 1 October 1999
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 883 (1) , 477-480
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Charcot-Marie-Tooth disease type 2 and P0 gene mutationsNeurology, 1999
- Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero geneNeurology, 1998
- A family presenting with electrophysiological ‘CMT type II’ and linked to Po geneNeuromuscular Disorders, 1997
- Heterozygous P0 Knockout Mice Develop a Peripheral Neuropathy that Resembles Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)Journal of Neuropathology & Experimental Neurology, 1997
- Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital HypomyelinationNeuron, 1996
- Protein zero (P0)–deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathiesNature Genetics, 1995
- HMSN III phenotype due to homozygous expression of a dominant HMSN II geneNeurology, 1992