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人红细胞磷酸葡萄糖变位酶(PGM1)的等电聚焦。托斯卡纳人群中的表型分布及两种遗传变异型

Isoelectric focusing of human red cell phosphoglucomutase (PGM1). Phenotype distribution in the population of Tuscany and two hereditary variants.

作者信息

Bargagna M, Abbagnale L

出版信息

Hum Genet. 1982;61(3):242-5. doi: 10.1007/BF00296450.

Abstract

Phosphoglucomutase (PGM1) phenotypes were determined in a population sample of Tuscany, Italy, by isoelectric focusing. The frequencies observed for the four alleles are: PGM1+1 = 0.6012, PGM1-1 = 0.1059, PGM2+1 = 0.2495, PGM2-1 = 0.0434. Two variants were detected and it was possible to study the parentage of both of them. The pedigree of the propositus of the first variant shows that the variant occurs in combination with the common alleles PGM1 1+ and PGM1 2+ and that it has an autosomal dominant inheritance. The second variant has been shown to be a product of the PGM2 locus, although its PAGIF pattern is included between 2- and 1+ isoenzymes.

摘要

通过等电聚焦法在意大利托斯卡纳的人群样本中测定了磷酸葡萄糖变位酶(PGM1)的表型。观察到的四个等位基因的频率分别为:PGM1 +1 = 0.6012,PGM1 -1 = 0.1059,PGM2 +1 = 0.2495,PGM2 -1 = 0.0434。检测到两个变体,并且有可能对它们两者的亲本关系进行研究。第一个变体先证者的家系表明,该变体与常见等位基因PGM1 1+和PGM1 2+同时出现,并且具有常染色体显性遗传。第二个变体已被证明是PGM2基因座的产物,尽管其PAGIF模式介于2-和1+同工酶之间。

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