Børresen A L, Jordfald A B, Berg K
Clin Genet. 1985 Apr;27(4):411-3. doi: 10.1111/j.1399-0004.1985.tb02285.x.
Restriction fragment length polymorphisms detectable with the RC8 probe, a probe for an area located on the short arm of the X-chromosome, and loosely linked to the locus for Duchenne muscular dystrophy, have been studied in a Norwegian population. With the TaqI enzyme three variants were observed. The gene frequencies of the previously detected variants were 0.867 and 0.082, respectively, and the frequency of a new variant was 0.051. Family studies confirmed Mendelian inheritance of the variants.
利用RC8探针(一种针对位于X染色体短臂上的一个区域的探针,与杜兴氏肌营养不良症的基因座松散连锁)可检测到的限制性片段长度多态性,已在挪威人群中进行了研究。使用TaqI酶观察到了三种变体。先前检测到的变体的基因频率分别为0.867和0.082,一种新变体的频率为0.051。家系研究证实了这些变体的孟德尔遗传方式。