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哥斯达黎加的苯丙酮尿症:苯丙氨酸羟化酶基因突变的初步谱及其与高度多态性单倍型的关联

Phenylketonuria in Costa Rica: preliminary spectrum of PAH mutations and their associations with highly polymorphic haplotypes.

作者信息

Santos M, Kuzmin A I, Eisensmith R C, Goltsov A A, Woo S L, Barrantes R, de Céspedes C

机构信息

INISA, Universidad de Costa Rica, San Jose, Costa Rica.

出版信息

Hum Hered. 1996 May-Jun;46(3):128-31. doi: 10.1159/000154340.

Abstract

A preliminary evaluation of the molecular basis of phenylketonuria (PKU) in Costa Rica was made by performing mutational analyses in the six PKU families identified to date. These studies revealed the presence of the previously reported European mutations IVS1nt5, L48S, E221G and IVS12ntl as well as the novel mutation IVS7nt3. The combined use of the STR, VNTR and XmnI polymorphic systems for the PAH gene resulted in a discriminant distribution of haplotypes among normal and mutant chromosomes and suggests its potential usefulness for future diagnostic applications in Costa Rican PKU kindreds. This is the first report of a genetic analysis in a Central American PKU population.

摘要

通过对哥斯达黎加迄今确定的6个苯丙酮尿症(PKU)家系进行突变分析,对PKU的分子基础进行了初步评估。这些研究揭示了先前报道的欧洲突变IVS1nt5、L48S、E221G和IVS12ntl的存在,以及新的突变IVS7nt3。PAH基因的STR、VNTR和XmnI多态性系统的联合使用导致单倍型在正常和突变染色体之间呈现判别性分布,并表明其在哥斯达黎加PKU家系未来诊断应用中的潜在用途。这是中美洲PKU人群遗传分析的首次报告。

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