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- W2008746087 abstract "The human neurological channelopathies are a rapidly expanding group of mainly genetic conditions that are characterized by dysfunction of membrane-bound glycoproteins (ion channels). The skeletal muscle channelopathies were the first to be characterized in this group. In recent years significant progress has been made in our understanding of the molecular genetic and cellular electrophysiological bases of these disorders. DNA-based diagnosis is now a reality for many of the channelopathies. The advances made have implications for both genetic counselling and for tailoring treatment to specific channelopathies." @default.
- W2008746087 created "2016-06-24" @default.
- W2008746087 creator A5009171206 @default.
- W2008746087 creator A5069214838 @default.
- W2008746087 date "2001-10-01" @default.
- W2008746087 modified "2023-09-25" @default.
- W2008746087 title "The skeletal muscle channelopathies: basic science, clinical genetics and treatment" @default.
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- W2008746087 doi "https://doi.org/10.1097/00019052-200110000-00001" @default.
- W2008746087 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11562564" @default.
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