Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness
- 20 September 2000
- journal article
- research article
- Published by Wiley in Muscle & Nerve
- Vol. 23 (10) , 1508-1514
- https://doi.org/10.1002/1097-4598(200010)23:10<1508::aid-mus6>3.0.co;2-d
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I lociNeurology, 2000
- Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22Neurology, 1999
- Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.Journal of Neurology, Neurosurgery & Psychiatry, 1997
- The gene for hereditary sensory neuropathy type I (HSN–I) maps to chromosome 9q22.1–q22.3Nature Genetics, 1996
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Avoiding Recomputation in Linkage AnalysisHuman Heredity, 1994
- Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic HeterogeneityGenomics, 1993
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984
- SEVERE SENSORY CHANGES, AND TROPHIC DISORDER, IN PERONEAL MUSCULAR ATROPHY (CHARCOT-MARIE-TOOTH TYPE)Archives of Neurology & Psychiatry, 1952
- HEREDITARY SENSORY RADICULAR NEUROPATHYJournal of Neurology, Neurosurgery & Psychiatry, 1951