Alestrøm A, Fagerlund T H, Berg K
Institute of Medical Genetics, University of Oslo, Norway.
Clin Genet. 1995 May;47(5):274-5. doi: 10.1111/j.1399-0004.1995.tb04311.x.
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.
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。