Phenotypic variability of autosomal dominant myotonia congenita in a Taiwanese family with muscle chloride channel (CLCN1) mutation.

Chang, Ting-Yu

Phenotypic variability of autosomal dominant myotonia congenita in a Taiwanese family with muscle chloride channel (CLCN1) mutation. [electronic resource] - Acta neurologica Taiwanica Dec 2007 - 214-20 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1028-768X


Adolescent
Aged
Chloride Channels--genetics
Electromyography
Female
Genes, Dominant
Humans
Male
Middle Aged
Mutation
Myotonia Congenita--genetics
Phenotype