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在囊性纤维化跨膜传导调节因子(CFTR)基因中检测到的突变和序列变异:来自囊性纤维化遗传分析联盟的报告。

Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium.

作者信息

Tsui L C

机构信息

Department of Genetics, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Hum Mutat. 1992;1(3):197-203. doi: 10.1002/humu.1380010304.

Abstract

Cystic fibrosis is the most common autosomal disorder in the Caucasian population. Since the description of the major mutation of this disease in 1989, over 150 of additional mutations have been identified in the CFTR gene. This update summarizes the different mutations identified and reported before March 15 by members of the international Cystic Fibrosis Genetic Analysis Consortium. The report includes information on DNA sequence variations found in the gene.

摘要

囊性纤维化是白种人群中最常见的常染色体疾病。自1989年描述了该疾病的主要突变以来,在囊性纤维化跨膜传导调节因子(CFTR)基因中又发现了150多种其他突变。本更新总结了国际囊性纤维化遗传分析联盟成员在3月15日前鉴定和报告的不同突变。该报告包括该基因中发现的DNA序列变异信息。

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