Diagnostic criteria for autosomal dominant hereditary motor and sensory neuropathy type Ia
- 31 December 1993
- journal article
- research article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 3 (1) , 77-79
- https://doi.org/10.1016/0960-8966(93)90045-l
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1ANature Genetics, 1992
- The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplicationNature Genetics, 1992
- The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1ANature Genetics, 1992
- The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1ANature Genetics, 1992
- Trembler mouse carries a point mutation in a myelin geneNature, 1992
- Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene regionHuman Genetics, 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