Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease
- 18 January 2000
- journal article
- clinical trial
- Published by Wiley in Muscle & Nerve
- Vol. 23 (2) , 182-188
- https://doi.org/10.1002/(sici)1097-4598(200002)23:2<182::aid-mus6>3.0.co;2-w
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- X-linked Charcot-Marie-Tooth disease with connexin 32 mutationsNeurology, 1998
- Altered Trafficking of Mutant Connexin32Journal of Neuroscience, 1997
- Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32Journal of Neuroscience, 1997
- Electrophysiological studies in the different genotypes of Charcot-Marie-Tooth diseaseCurrent Opinion in Neurology, 1996
- Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth diseaseNeuron, 1994
- Connexin Mutations in X-Linked Charcot-Marie-Tooth DiseaseScience, 1993
- Inherited Primary Peripheral NeuropathiesPublished by American Medical Association (AMA) ,1993
- Screening of dominantly inherited Charcot–Marie–Tooth neuropathiesMuscle & Nerve, 1993
- The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathiesNeurology, 1982
- Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular AtrophyArchives of Neurology, 1968