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苯丙氨酸羟化酶(PAH)基因座的分子变异分析。

Analysis of the molecular variance at the phenylalanine hydroxylase (PAH) locus.

作者信息

Degioanni A, Darlu P

机构信息

Istituto di Genetica Biochimica ed Evoluzionistica, Pavia, Italy.

出版信息

Eur J Hum Genet. 1994;2(3):166-76. doi: 10.1159/000472360.

Abstract

The frequencies of the different haplotypes identified at the phenylalanine hydroxylase (PAH) locus were analyzed for both phenylketonuria (PKU) and normal haplotypes of various European, Asiatic, Polynesian and Black American populations. These molecular variants were studied by applying a specific model of multivariate analysis of variance, allowing an estimation of components of variance at different levels of hierarchical subdivisions (intrapopulation, among different geographical groups of populations, and between PKU and normal haplotypes within populations). The results indicate that the PAH polymorphism could be appropriate to study divergence between African, European and Asiatic population groups, but is not sufficient to explain the diversity among European populations. However, the differences in PAH haplotype frequencies between PKU and normal haplotypes are statistically significant over all European populations.

摘要

对欧洲、亚洲、波利尼西亚和美国黑人等不同人群中苯丙酮尿症(PKU)和正常单倍型在苯丙氨酸羟化酶(PAH)基因座上鉴定出的不同单倍型频率进行了分析。通过应用特定的多变量方差分析模型对这些分子变异进行研究,从而能够估计不同层次细分水平(群体内部、不同地理群体之间以及群体内PKU和正常单倍型之间)的方差成分。结果表明,PAH多态性可能适合用于研究非洲、欧洲和亚洲人群组之间的差异,但不足以解释欧洲人群内部的多样性。然而,在所有欧洲人群中,PKU和正常单倍型之间PAH单倍型频率的差异具有统计学意义。

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