Ramus S J, Cotton R G
Olive Miller Protein Laboratory, Murdoch Institute, Royal Children's Hospital, Parkville, Melbourne, Victoria, Australia.
Hum Genet. 1995 Dec;96(6):741-3. doi: 10.1007/BF00210312.
A polymorphism was identified in 3' untranslated region of the phenylalanine hydroxylase gene using the newly described mutation detection method, enzyme mismatch cleavage. This polymorphism, 1546 G-->A, was linked to three mutations on several haplotype backgrounds. A group of haplotypes was identified as evolving from the one ancestral haplotype on which this base substitution occurred. The possible Celtic or Viking origin of this polymorphism is discussed.
使用新描述的突变检测方法——酶错配切割,在苯丙氨酸羟化酶基因的3'非翻译区鉴定出一种多态性。这种多态性,即1546 G→A,在几种单倍型背景下与三个突变相关联。一组单倍型被确定为由发生该碱基替换的一个祖先单倍型进化而来。本文讨论了这种多态性可能的凯尔特或维京起源。