Genetic Refinement and Physical Mapping of the CMT4B Gene on Chromosome 11q22
- 1 January 2000
- Vol. 63 (2), 271-278
- https://doi.org/10.1006/geno.1999.6088
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotypeBrain, 1999
- A Physical Map of 30,000 Human GenesScience, 1998
- Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)Neurology, 1998
- How to get the best of dbESTTrends in Genetics, 1998
- Hereditary demyelinating neuropathy of infancy: a genetically complex syndromeBrain, 1997
- Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth diseaseNeurology, 1996
- Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharingHuman Molecular Genetics, 1996
- Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qHuman Molecular Genetics, 1993
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction.Proceedings of the National Academy of Sciences, 1990