2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2–HMSN II) and Distal Hereditary Motor Neuropathy (Distal HMN–Spinal CMT)
- 1 August 1998
- journal article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 8 (6) , 426-431
- https://doi.org/10.1016/s0960-8966(98)00025-x
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.Journal of Neurology, Neurosurgery & Psychiatry, 1997
- A new type of hereditary motor and sensory neuropathy linked to chromosome 3Annals of Neurology, 1997
- Hereditary Motor and Sensory Neuropathy IIBNeurology, 1997
- Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D)Human Molecular Genetics, 1996
- The gene for hereditary sensory neuropathy type I (HSN–I) maps to chromosome 9q22.1–q22.3Nature Genetics, 1996
- Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2Neurology, 1996
- A Locus for Axonal Motor-Sensory Neuropathy with Deafness and Mental Retardation Maps to Xq24–q26Genomics, 1995
- Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic HeterogeneityGenomics, 1993
- Population frequencies of inherited neuromuscular diseases—A world surveyNeuromuscular Disorders, 1991
- Genetic and clinical aspects of Charcot‐Marie‐Tooth's diseaseClinical Genetics, 1974