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

By: Contributor(s): Producer: 20080215Description: 214-20 p. digitalISSN:
  • 1028-768X
Subject(s): In: Acta neurologica Taiwanica vol. 16
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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