首页 | 本学科首页   官方微博 | 高级检索  
     


A simple method to detect the RYR1 mutation G1021A, a cause of malignant hyperthermia susceptibility
Authors:A. Alestrø  m,T. H. Fagerlund,K. Berg
Affiliation:Institute of Medical Genetics, University of Oslo, Norway;Department of Anaesthesiology, Ullevål University Hospital, Oslo, Norway
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.
Keywords:ACRS technique    calcium release channel    DNA    genetics    human mutation    malignant hyperthermia    RYR1
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号