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Linkage disequilibrium between DNA polymorphisms within the porphobilinogen deaminase gene.

作者信息

Scobie G A, Urquhart A J, Elder G H, Kalsheker N A, Llewellyn D H, Smyth J, Harrison P R

机构信息

Department of Medical Biochemistry, University of Wales College of Medicine, Heath Park, Cardiff, UK.

出版信息

Hum Genet. 1990 Jul;85(2):157-9. doi: 10.1007/BF00193188.

Abstract

Three restriction fragment length polymorphisms (RFLPs) (MspI, PstI, ScrFI/BstNI) within the human porphobilinogen deaminase (PBG-D) gene have been studied in 47 unrelated patients with the autosomal dominant disorder, acute intermittent porphyria (AIP), and in 92 control subjects. Each enzyme identified a two-allele polymorphism with allele frequencies close to 0.50: however, marked linkage disequilibrium limited the number of observed haplotypes to four, of which one is uncommon. No association was detected between any haplotype and AIP.

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