Hypoxanthine-guanine phosphoribosyltransferase gene analysis for Japanese patients with Lesch-Nyhan syndrome
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.1996.tb03432.x/fullpdf
Reference23 articles.
1. A familial disorder of uric acid metabolism and central nervous system function;Lesch;Am. J. Med.,1964
2. Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis;Seegmiller;Science,1967
3. The HGPRT locus;Casky;Cell,1979
4. Cloned cDNA sequences of the hypoxanthine-guanine phosphoribosyltransferase gene from a mouse neuroblastoma cell line found to have amplified genomic sequences;Brennand;Proc. Natl Acad. Sci.,1982
5. Isolation and characterization of full-length expressible cDNA for human hypoxanthine phosphoribosyltransferase;Jolly;Proc. Natl Acad. Sci.,1983
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