Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease. [electronic resource]
Producer: 20040601Description: 361-70 p. digitalISSN:- 0969-9961
- Amino Acid Substitution
- Animals
- Axons -- metabolism
- Cell Membrane -- genetics
- Cells, Cultured
- Charcot-Marie-Tooth Disease -- genetics
- Connexins -- genetics
- Demyelinating Diseases -- genetics
- Gap Junctions -- genetics
- Genes, Dominant
- Genetic Diseases, X-Linked -- genetics
- Humans
- Ion Channels -- genetics
- Membrane Potentials -- genetics
- Mice
- Mutation -- genetics
- Patch-Clamp Techniques
- Schwann Cells -- metabolism
- Gap Junction beta-1 Protein
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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