Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot–Marie–Tooth disease
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Neuroscience
Reference65 articles.
1. Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene;Ainsworth;Hum. Genet.,1998
2. Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32;Anzini;J. Neurosci.,1997
3. Central visual, acoustic, and motor pathway involvement in a Charcot–Marie–Tooth family with an Asn205Ser mutation in the connexin32 gene;Bahr;J. Neurol. Neurosurg. Psychiatry,1999
4. Functional gap junctions in the schwann cell myelin sheath;Balice-Gordon;J. Cell. Biol.,1998
5. Structure–function studies of voltage sensitivity of connexins, the family of gap junction forming proteins;Bennett;Jpn,1993
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