| Literature DB >> 1973402 |
G A Scobie1, A J Urquhart, G H Elder, N A Kalsheker, D H Llewellyn, J Smyth, P R Harrison.
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.Entities:
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Year: 1990 PMID: 1973402 DOI: 10.1007/bf00193188
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132