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常染色体显性多囊肾病的第二个基因位点。

A second genetic locus for autosomal dominant polycystic kidney disease.

作者信息

Romeo G, Devoto M, Costa G, Roncuzzi L, Catizone L, Zucchelli P, Germino G G, Keith T, Weatherall D J, Reeders S T

机构信息

Laboratorio di Genetica Molecolare, Istituto G. Gaslini, Genoa, Italy.

出版信息

Lancet. 1988 Jul 2;2(8601):8-11. doi: 10.1016/s0140-6736(88)92943-1.

Abstract

Hitherto, mutations that lead to autosomal dominant adult-type polycystic kidney disease have been found to be linked to the alpha-globin genes on the short arm of chromosome 16. In an Italian family, absence of linkage between the disease mutation and alpha-globin indicates that the condition can be caused by mutations in a second gene. The clinical features of the disease in this Italian family are indistinguishable from those found in the "linked" families. The finding that there are two polycystic kidney disease genes means that linkage must be demonstrated independently in each family before predictive tests with DNA probes can be used reliably.

摘要

迄今为止,已发现导致常染色体显性成人型多囊肾病的突变与16号染色体短臂上的α-珠蛋白基因有关。在一个意大利家族中,疾病突变与α-珠蛋白之间不存在连锁关系,这表明该病可能由另一个基因的突变引起。这个意大利家族中该疾病的临床特征与那些“连锁”家族中发现的特征并无差异。存在两种多囊肾病基因这一发现意味着,在能够可靠地使用DNA探针进行预测性检测之前,必须在每个家族中独立证明连锁关系。

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