Partial phenotypic correction of human Lesch-Nyhan (hypoxanthine-guanine phosphoribosyltransferase-deficient) lymphoblasts with a transmissible retroviral vector.-Reference-Cited by-同舟云学术

Partial phenotypic correction of human Lesch-Nyhan (hypoxanthine-guanine phosphoribosyltransferase-deficient) lymphoblasts with a transmissible retroviral vector.

Published:1984-06 Issue:12 Volume:259 Page:7842-7849
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Willis R C,Jolly D J,Miller A D,Plent M M,Esty A C,Anderson P J,Chang H C,Jones O W,Seegmiller J E,Friedmann T

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference54 articles.

1. A familial disorder of uric acid metabolism and central nervous system function

2. Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

3. A specific enzyme defect in gout associated with overproduction of uric acid.

4. Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency in Gout

5. A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

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