Genetic basis of hypoxanthine guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome (HPRTFlint) [PDF]
Beverly L. Davidson+3 more
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Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndrome. [PDF]
Shin Fujimori+3 more
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Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in thirteen Spanish families [PDF]
Rosa J. Torres+7 more
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Human hypoxanthine-guanine phosphoribosyltransferase: a single nucleotide substitution in cDNA clones isolated from a patient with Lesch-Nyhan syndrome (HPRTMidland) [PDF]
Beverly L. Davidson+2 more
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The development of hypoxanthine-guanine phosphoribosyltransferase activity in man [PDF]
R A Harkness+3 more
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Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjects. [PDF]
Beverly L. Davidson+4 more
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Chinese Hamster Hypoxanthine-Guanine Phosphoribosyltransferase
Anne S. Olsen, Gregory Milman
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Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene [PDF]
Herdis Steingrimsdottir+4 more
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Human hypoxanthine-guanine phosphoribosyltransferase. Evidence for tetrameric structure.
J A Holden, William N. Kelley
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Functional characterization of the human hypoxanthine phosphoribosyltransferase gene promoter: evidence for a negative regulatory element. [PDF]
Diego E. Rincón-Limas+2 more
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