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红细胞尿苷单磷酸激酶和氨基乙酰丙酸脱水酶的基因分析及其在亲子鉴定中的应用。

Genetic analysis of erythrocyte uridine monophosphate kinase and aminolevulinate dehydrase and its application to paternity testing.

作者信息

Caeiro J L, Llano C, Garcia-Luengo S, Canabal O

机构信息

Faculty of Biology, University of Santiago de Compostela, Galicia, Spain.

出版信息

J Forensic Sci. 1989 Sep;34(5):1090-4.

PMID:2553853
Abstract

Simultaneous determination of uridine monophosphate kinase (UMPK) and aminolevulinate dehydrase (ALAD) has been carried out after discontinuous starch gel electrophoresis in the Galician population (NW Spain), including 129 families with a total of 291 descendents. Formal genetic studies are in agreement with the autosomal codominant way of inheritance for each locus. No evidence of phenotype association between both loci among the offspring is observed. Chance of exclusion for non-fathers is 0.041 13 for UMPK and 0.0702 for ALAD configuring a total exclusion rate of 0.1085 when both systems are evaluated together.

摘要

在加利西亚人群(西班牙西北部)中,通过不连续淀粉凝胶电泳同时测定了尿苷单磷酸激酶(UMPK)和氨基乙酰丙酸脱水酶(ALAD),该人群包括129个家庭,共有291名后代。正式的遗传学研究与每个基因座的常染色体共显性遗传方式相符。在后代中未观察到两个基因座之间存在表型关联的证据。UMPK的非父排除几率为0.041 13,ALAD为0.0702,当两个系统一起评估时,总排除率为0.1085。

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