Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population

被引:64
作者
Li, L
Eng, C
Desnick, RJ
German, J
Ellis, NA
机构
[1] CUNY Mt Sinai Sch Med, Dept Human Genet, New York, NY 10029 USA
[2] New York Blood Ctr, Lab Human Genet, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Human Genet, New York, NY 10021 USA
关键词
Bloom syndrome; Jewish genetic disease; founder effect; carrier screening; genetic testing;
D O I
10.1006/mgme.1998.2733
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bloom syndrome is more common in individuals of Ashkenazi Jewish descent than in any other population, and one particular mutation in the Bloom syndrome gene, blm(Ash), is homozygous in nearly all Ashkenazi Jewish persons with Bloom syndrome. We have determined the frequency of blm(Ash) in 1491 Ashkenazi Jewish persons with no known history of Bloom syndrome and found that 1 in 107 persons was heterozygous. Although not common, genetic screening for Bloom syndrome is feasible in this population, (C) 1998 Academic Press.
引用
收藏
页码:286 / 290
页数:5
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