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Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

โœ Scribed by Fontaine, B; Khurana, T.; Hoffman, E.; Bruns, G.; Haines, J.; Trofatter, J.; Hanson, M.; Rich, J; McFarlane, H; Yasek, D.; et, al.


Book ID
123611785
Publisher
American Association for the Advancement of Science
Year
1990
Tongue
English
Weight
773 KB
Volume
250
Category
Article
ISSN
0036-8075

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Hyperkalemic periodic paralysis (HPP) is caused by mutations of the adult skeletal muscle sodium channel (SCN4A) gene on chromosome 17. Malignant hyperthermia (MH) is a genetically heterogeneous autosomal-dominant disorder occurring in association with various neuromuscular diseases or without other