A simple method to detect the RYR1 mutation G1021A, a cause of malignant hyperthermia susceptibility |
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Authors: | A. Alestrø m,T. H. Fagerlund,K. Berg |
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Affiliation: | Institute of Medical Genetics, University of Oslo, Norway;Department of Anaesthesiology, Ullevål University Hospital, Oslo, Norway |
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Abstract: | To search for the mutations RYR1 G1021A in families where malignant hyperthermia (MH) episodes have occurred, we have used an amplificationcreated restriction sites (ACRS) technique to detect the mutation. The previously described single-stranded conformation polymorphism (SSCP) technique was laborious and time consuming, but necessary to detect the mutation, whereas the method described here discriminates quickly and efficiently between homozygotes with the mutation, heterozygotes and homozygotes without the mutation. |
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Keywords: | ACRS technique calcium release channel DNA genetics human mutation malignant hyperthermia RYR1 |
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