2000•Molecular Brain ResearchRequires access

Point mutation associated with X-linked dominant Charcot-Marie-Tooth disease impairs the P2 promoter activity of human connexin-32 gene

H.-L. Wang, Tony Wu, Wei‐Ting Chang, A.H. Li, M.-S. Chen, Ching‐Yi Wu, W. Fang

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Key concepts: Connexin, Biology, Connexin 32, Gene, Point mutation, Peripheral myelin protein 22, Myelin, Mutation

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Point mutation associated with X-linked dominant Charcot-Marie-Tooth disease impairs the P2 promoter activity of human connexin-32 gene — Research Paper | ScholarLens