Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing. [electronic resource]
Producer: 20011204Description: 461-8 p. digitalISSN:- 1107-3756
- Adolescent
- Adult
- Base Sequence
- Blinking -- physiology
- Brain Stem -- physiopathology
- Charcot-Marie-Tooth Disease -- genetics
- Connexins -- genetics
- DNA -- chemistry
- DNA Mutational Analysis
- Evoked Potentials, Auditory, Brain Stem -- physiology
- Evoked Potentials, Visual -- physiology
- Family Health
- Female
- Genetic Linkage
- Humans
- Male
- Mutation
- Mutation, Missense
- Neural Conduction -- physiology
- Pedigree
- Peripheral Nerves -- physiopathology
- Reflex -- physiology
- X Chromosome -- genetics
- Gap Junction beta-1 Protein
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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