MAPPING OF THE AUTOSOMAL-DOMINANT EXUDATIVE VITREORETINOPATHY LOCUS (EVR1) BY MULTIPOINT LINKAGE ANALYSIS IN 4 FAMILIES

被引:17
作者
MULLER, B
ORTH, U
VANNOUHUYS, CE
DUVIGNEAU, C
FUHRMANN, C
SCHWINGER, E
LAQUA, H
GAL, A
机构
[1] MED UNIV LUBECK,INST HUMANGENET,RATZEBURGER ALLEE 160,D-23538 LUBECK,GERMANY
[2] MED UNIV LUBECK,AUGENKLIN,D-23538 LUBECK,GERMANY
[3] UNIV MUNICH,KINDERPOLIKLIN,PADIAT GENET ABT,W-8000 MUNICH 2,GERMANY
[4] CW HOSP,DEPT OPHTHALMOL,NIJMEGEN,NETHERLANDS
关键词
D O I
10.1006/geno.1994.1176
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Autosomal dominant exudative vitreoretinopathy is a disorder affecting primarily the development of the human retinal vascular system. The disease locus has recently been assigned to 11q13-q23 by linkage studies in two families. Two-point analysis on a total of four families has now revealed close linkage (z(max) = 8.34 at theta = 0.00) between the disease locus and D11S873. Multipoint linkage analysis mapped the disease locus between D11S527/D11S533 and D11S35 with a maximum lod score of over 11 directly at D11S873. No evidence appeared for genetic/linkage heterogeneity among the four families examined. (C) 1994 Academic Press, Inc.
引用
收藏
页码:317 / 319
页数:3
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