Complete identification of cystic fibrosis transmembrane conductance regulator mutations in the CF population of Saguenay Lac-Saint-Jean (Quebec, Canada)

被引:20
作者
De Braekeleer, M
Mari, C
Verlingue, C
Allard, C
Leblanc, JP
Simard, F
Aubin, G
Ferec, C
机构
[1] Univ Quebec, Dept Sci Humaines, Lab Rech Fibrose Kyst, Quebec City, PQ G7H 2B1, Canada
[2] Hop Chicoutimi, Clin Fibrose Kyst, Quebec City, PQ, Canada
[3] Etab Transfus Sanguine Bretagne Occidentale, Brest, France
关键词
denaturing gradient gel electrophoresis; CFTR mutations; cystic fibrosis; prevalence; French Canadian;
D O I
10.1034/j.1399-0004.1998.531530108.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Over the past few years, we have conducted a systematic study of 230 cystic fibrosis (CF) chromosomes in the Saguenay Lac-Saint-Jean (SLSJ) population which has a high CF incidence (1/936 live births). We identified 11 mutations accounting for 100% of the CF chromosomes found in patients born in SLSJ, Our results indicate that denaturing gradient gel electrophoresis (DGGE) is a powerful method of identifying CF mutations, They have also considerable implications for genetic counselling and molecular characterization of doubtful patients. They make carrier screening technically feasible in this population.
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页码:44 / 46
页数:3
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