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一种检测导致恶性高热易感性的RYR1突变G1021A的简单方法。

A simple method to detect the RYR1 mutation G1021A, a cause of malignant hyperthermia susceptibility.

作者信息

Alestrøm A, Fagerlund T H, Berg K

机构信息

Institute of Medical Genetics, University of Oslo, Norway.

出版信息

Clin Genet. 1995 May;47(5):274-5. doi: 10.1111/j.1399-0004.1995.tb04311.x.

Abstract

To search for the mutations RYR1 G1021A in families where malignant hyperthermia (MH) episodes have occurred, we have used an amplification-created 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.

摘要

为了在发生恶性高热(MH)发作的家族中寻找RYR1 G1021A突变,我们采用了扩增产生限制位点(ACRS)技术来检测该突变。先前描述的单链构象多态性(SSCP)技术既费力又耗时,但对于检测该突变是必要的,而此处描述的方法能够快速、有效地区分携带突变的纯合子、杂合子和不携带突变的纯合子。

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