Charcot-Marie-tooth disease: a new paradigm for the mechanism of inherited disease
- 30 April 1994
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 10 (4) , 128-133
- https://doi.org/10.1016/0168-9525(94)90214-3
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- De-novo mutation in hereditary motor and sensory neuropathy type IThe Lancet, 1992
- Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot‐Marie‐Tooth disease type 1)Annals of Neurology, 1992
- Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.Journal of Medical Genetics, 1992
- Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families.Journal of Medical Genetics, 1992
- DNA duplication associated with Charcot-Marie-Tooth disease type 1ACell, 1991
- Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)Neuromuscular Disorders, 1991
- Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17Experimental Neurology, 1989
- Indomethacin in the treatment of lithium-induced nephrogenic diabetes insipidusArchives of internal medicine (1960), 1989
- X-linked dominant Charcot-Marie-Tooth disease: Suggestion of linkage with a cloned DNA sequence from the proximal XqHuman Genetics, 1985
- Genetic and clinical aspects of Charcot‐Marie‐Tooth's diseaseClinical Genetics, 1974