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    Genomics. 1991 Jun;10(2):499-501.

    Determination of the mutations responsible for the Lesch-Nyhan syndrome in 17 subjects.

    Tarlé SA, Davidson BL, Wu VC, Zidar FJ, Seegmiller JE, Kelley WN, Palella TD.

    Department of Internal Medicine, Rackham Arthritis Research Unit, University of Michigan, Ann Arbor 48109.

    Hypoxanthine--guanine phosphoribosyltransferase (HPRT) is a purine salvage enzyme that catalyzes the conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate. Previous studies of mutant HPRT proteins analyzed at the molecular level have shown a significant heterogeneity. This investigation further verifies this heterogeneity and identifies insertions, deletions, and point mutations. The direct sequencing of the polymerase chain reaction-amplified product of reverse-transcribed HPRT mRNA enabled the rapid identification of the mutations found in 17 previously uncharacterized cell lines derived from patients with the Lesch-Nyhan syndrome.

    PMID: 2071157 [PubMed - indexed for MEDLINE]

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