A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21
- 30 August 2001
- journal article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 9 (8) , 646-650
- https://doi.org/10.1038/sj.ejhg.5200686
Abstract
The European Journal of Human Genetics is the official Journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports, News and Commentary articles and reviews in the rapidly expanding field of human genetics and genomics.Keywords
This publication has 7 references indexed in Scilit:
- Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2EAnnals of Neurology, 2001
- Periaxin Mutations Cause Recessive Dejerine-Sottas NeuropathyAmerican Journal of Human Genetics, 2001
- N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–LomAmerican Journal of Human Genetics, 2000
- A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light GeneAmerican Journal of Human Genetics, 2000
- Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2Nature Genetics, 2000
- Hereditary Peripheral NeuropathiesPublished by S. Karger AG ,2000
- Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathiesHuman Mutation, 1999