Histopathological features of X-linked Charcot-Marie-Tooth disease in 8 patients from 6 families with different connexin32 mutations
- 7 July 2008
- journal article
- Published by Wiley in Journal of the Peripheral Nervous System
- Vol. 6 (2) , 79-84
- https://doi.org/10.1111/j.1529-8027.2001.01011.x
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth diseaseMuscle & Nerve, 2000
- The challenge of CMTX and connexin 32 mutationsMuscle & Nerve, 2000
- Peripheral myelin modification in CMT1B correlates with MPZ gene mutationsNeuromuscular Disorders, 1999
- Genotype/Phenotype Correlations in X‐Linked Dominant Charcot‐Marie‐Tooth DiseaseAnnals of the New York Academy of Sciences, 1999
- X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutationsJournal of the Neurological Sciences, 1999
- A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and DeafnessAmerican Journal of Human Genetics, 1999
- The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotypeBrain, 1999
- X-linked Charcot-Marie-Tooth disease with connexin 32 mutationsNeurology, 1998
- Examination of the Peripheral Nerve BiopsyPublished by Elsevier ,1995
- Connexin Mutations in X-Linked Charcot-Marie-Tooth DiseaseScience, 1993