Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-tooth neuropathy
- 14 June 1996
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 63 (3) , 486-491
- https://doi.org/10.1002/(sici)1096-8628(19960614)63:3<486::aid-ajmg14>3.0.co;2-i
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- A linkage study of the locus for X-linked Charcot-Marie-Tooth diseaseClinical Genetics, 2008
- Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth diseaseNeuron, 1994
- Mutations in the connexin 32 gene in X-linked dominant Charcot- Marie - Tooth disease (CMTX1)Human Molecular Genetics, 1994
- Connexin Mutations in X-Linked Charcot-Marie-Tooth DiseaseScience, 1993
- Mutational analysis of gap junction formationBiophysical Journal, 1992
- Linkage in a family with X-linked Charcot-Marie-Tooth diseaseClinical Genetics, 1989
- X‐linked dominant charcot–marie–tooth neuropathy with 15 cases in a family genetic linkage studyMuscle & Nerve, 1988
- X‐linked neuropathy: Gene localization with DNA probesAnnals of Neurology, 1986
- X-linked dominant Charcot-Marie-Tooth disease: Suggestion of linkage with a cloned DNA sequence from the proximal XqHuman Genetics, 1985
- Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular AtrophyArchives of Neurology, 1968