期刊
JOURNAL OF NEUROLOGY
卷 249, 期 11, 页码 1493-1502出版社
DR DIETRICH STEINKOPFF VERLAG
DOI: 10.1007/s00415-002-0871-5
关键词
ionchannels; hereditary diseases; sodium; potassium; calcium chloride
Ion channelopathies have common clinical features, recurrent patterns of mutations, and almost predictable mechanisms of pathogenesis. In skeletal muscle, disorders are associated with mutations in voltage-gated Na+, K+, Ca2+, and Cl- channels leading to hypoexcitability, causing periodic paralysis and to hyperexcitabilty, resulting in myotonia or susceptibility to malignant hyperthermia.
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