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一个泰人家族中的β0地中海贫血是由一个3.4 kb的缺失引起的,该缺失包括整个β珠蛋白基因。

Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.

作者信息

Sanguansermsri T, Pape M, Laig M, Hundrieser J, Flatz G

机构信息

Human Genetics Unit, Faculty of Medicine, Chiangmai University, Thailand.

出版信息

Hemoglobin. 1990;14(2):157-68. doi: 10.3109/03630269009046957.

Abstract

DNA analysis of a Northern Thai family with a child affected with beta-thalassemia major revealed a novel deletion of 3.4 kb removing the entire beta-globin gene in the proposita and her mother. Detailed mapping of the deletion located the 5' breakpoint in the region between nucleotides -810 and -128 of the beta-globin locus, and the 3' breakpoint between the Ava II and Xmn I sites located downstream of the beta-globin gene. The father transmitted a codon 17 nonsense mutation, a beta-thalassemia variant common in Thailand, to the child.

摘要

对一个来自泰国北部、有一个重型β地中海贫血患儿的家庭进行的DNA分析显示,先证者及其母亲存在一种新的3.4 kb缺失,该缺失移除了整个β珠蛋白基因。对该缺失进行详细定位发现,5'断点位于β珠蛋白基因座核苷酸-810和-128之间的区域,3'断点位于β珠蛋白基因下游的Ava II和Xmn I位点之间。父亲将一个17密码子无义突变(泰国常见的一种β地中海贫血变异型)遗传给了孩子。

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