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五个患有莱施-奈恩综合征的韩国家庭中次黄嘌呤鸟嘌呤磷酸核糖转移酶(HPRT)基因的分子分析。

Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) gene in five Korean families with Lesch-Nyhan syndrome.

作者信息

Kim K J, Yamada Y, Suzumori K, Choi Y, Yang S W, Cheong H I, Hwang Y S, Goto H, Ogasawara N

机构信息

Department of Pediatrics, Seoul National University, College of Medicine, Korea.

出版信息

J Korean Med Sci. 1997 Aug;12(4):332-9. doi: 10.3346/jkms.1997.12.4.332.

Abstract

Lesch-Nyhan syndrome is caused by the complete deficiency of hypoxanthine guanine phosphoribosyl-transferase (HPRT). By the analysis of genomic DNA and mRNA using the polymerase chain reaction (PCR) technique coupled with direct sequencing, five independent mutations in HPRT genes have been identified in Korean Lesch-Nyhan families. Two novel mutations and three previously reported mutations have been found in five independent families. Heterozygous carriers were detected in all the families, and prenatal diagnosis was carried out in two families.

摘要

莱施-奈恩综合征由次黄嘌呤鸟嘌呤磷酸核糖转移酶(HPRT)完全缺乏所致。通过聚合酶链反应(PCR)技术结合直接测序对基因组DNA和mRNA进行分析,在韩国莱施-奈恩家族中鉴定出HPRT基因的5个独立突变。在5个独立家族中发现了2个新突变和3个先前报道的突变。所有家族均检测到杂合子携带者,其中2个家族进行了产前诊断。

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