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通过酶错配切割检测苯丙氨酸羟化酶基因3'非翻译区的多态性:单倍型的演变

Polymorphism in the 3' untranslated region of the phenylalanine hydroxylase gene detected by enzyme mismatch cleavage: evolution of haplotypes.

作者信息

Ramus S J, Cotton R G

机构信息

Olive Miller Protein Laboratory, Murdoch Institute, Royal Children's Hospital, Parkville, Melbourne, Victoria, Australia.

出版信息

Hum Genet. 1995 Dec;96(6):741-3. doi: 10.1007/BF00210312.

Abstract

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.

摘要

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。

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