GENETIC-LINKAGE OF FAMILIAL OPEN-ANGLE GLAUCOMA TO CHROMOSOME-1Q21-Q31

被引:354
作者
SHEFFIELD, VC
STONE, EM
ALWARD, WLM
DRACK, AV
JOHNSON, AT
STREB, LM
NICHOLS, BE
机构
[1] UNIV IOWA HOSP & CLIN,DEPT OPHTHALMOL,IOWA CITY,IA 52242
[2] UNIV IOWA HOSP & CLIN,DEPT PEDIAT,IOWA CITY,IA 52242
关键词
D O I
10.1038/ng0593-47
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Glaucoma is a significant cause of blindness world wide. There is evidence to suggest that at least a subset of the disease is determined genetically. We studied 37 members of a family affected with an autosomal dominant form of juvenile open angle glaucoma and 22 were found to be affected. Linkage analysis using short tandem repeat markers mapped the disease-causing gene to chromosome 1q21-q31. Eight markers were significantly linked (Z(max) > 3.0) to the disease, with the highest lod score 6.5 (theta=0), provided by D1S212. The atrial natriuretic peptide (ANP)/receptor system has been proposed to have a role in glaucoma and one of the ANP receptor genes maps to chromosome 1q.
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页码:47 / 50
页数:4
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