4.4 Article

DHPLC mutation analysis of phenylketonuria

期刊

MOLECULAR GENETICS AND METABOLISM
卷 78, 期 3, 页码 205-210

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S1096-7192(02)00228-7

关键词

PAH gene; phenylketonuria; mutation analysis; DHPLC

向作者/读者索取更多资源

Denaturing high-performance liquid chromatography (DHPLC) is a sensitive and fast method for the detection of mutations which has been successfully used for mutation screening in several disease-related genes. Phenylketonuria (PKU, OMIM* 261600; McKusick 1986) is one of the most common autosomal recessive disorders in Europe. Mutations in the PAH gene mainly involve point mutations. In this study we report the successful use of DHPLC to analyse rapidly the complete coding sequence of the PAH gene in a total of 125 unrelated patients with PKU. (C) 2003 Elsevier Science (USA). All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据