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Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005
See this aricle in Pubmed

Article Abstract
Ryanodine receptor mutations are found in at least 25% of known MH susceptible individuals in North America. Mutation analysis has recently become available in the United States and is expected to play an integral role in the diagnosis of MH susceptibility in the future.
 
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anesthesia,general
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chromosome 19
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genetic neurologic disorders
genetic screening
hypercapnia
hyperthermia
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prevention of neurologic disorders
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