Suppr超能文献

囊性纤维化患者登记处中ΔF508基因型的异常分布。

An abnormal distribution of delta F508 genotypes in cystic fibrosis patient registries.

作者信息

Feingold J, Guilloud-Bataille M, De Crozes D

机构信息

Unité de Recherches d'Epidémiologie Génétique, INSERM Unité 155, Université Paris 7, France.

出版信息

Ann Genet. 1998;41(1):31-3.

PMID:9599649
Abstract

Delta F508 mutation of the CFTR gene is the most frequent deleterious allele involved in cystic fibrosis (CF). We have studied the distribution of the three genotypes, delta F508/delta F508, delta F508/x, x/x, in the American, Canadian and French data registries concerning CF; "x" represents the non-delta F508 mutations. In the three registries the observed distribution of the three genotypes differs from the expected one, calculated according to the Hardy and Weinberg equilibrium. Three factors could explain this discrepancy: Wahlund's effect, misinterpretation of the molecular diagnosis, or an ascertainment bias in relation with the severity of the disease. This last factor is the most likely.

摘要

囊性纤维化跨膜传导调节因子(CFTR)基因的ΔF508突变是导致囊性纤维化(CF)的最常见有害等位基因。我们研究了美国、加拿大和法国CF数据登记处中三种基因型ΔF508/ΔF508、ΔF508/x、x/x的分布情况;“x”代表非ΔF508突变。在这三个登记处中,三种基因型的观察分布与根据哈迪-温伯格平衡计算出的预期分布不同。有三个因素可以解释这种差异:瓦伦德效应、分子诊断的错误解读,或与疾病严重程度相关的确诊偏倚。最后一个因素是最有可能的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验