Key result
This review summarizes the current understanding of muscle sodium, calcium, and chloride channels and their role in the pathogenesis of myotonia and periodic paralysis.
Design
Review
Authors
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Enhances molecular insights into muscle channelopathies; leaves open clinical translation of mutation-specific therapies.
This review summarizes the relationship between ion channel mutations and disorders of muscle excitability, such as myotonia and periodic paralysis.
Robert L. Barchi (1997) conducted a review in Diseases of skeletal muscle (myotonia and periodic paralysis). Ion channel mutations was evaluated. This review summarizes the current understanding of muscle sodium, calcium, and chloride channels and their role in the pathogenesis of myotonia and periodic paralysis.
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