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Clinica Chimica Acta, ISSN 0009-8981, 09/2017, Volume 472, pp. 136 - 138
Journal Article
Journal Article
Journal Article
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 01/2002, Volume 22, Issue 2, pp. 669 - 679
Journal Article
Neuroscience Letters, ISSN 0304-3940, 03/2015, Volume 590, pp. 35 - 39
Transcriptomic studies of murine D3 embryonic stem (ES) cells deficient in the purinergic biosynthetic function hypoxanthine guanine phosphoribosyltransferase... 
Neurodegenerative disease | HPRT | Alzheimer’s disease | Neurogenesis | Neurodevelopment disease | Lesch–Nyhan disease
Journal Article
Nucleosides, Nucleotides and Nucleic Acids, ISSN 1525-7770, 12/2011, Volume 30, Issue 12, pp. 1260 - 1265
Hypoxanthine phosphoribosyltranferase (HPRT) deficiency is an X-linked disorder of purine salvage that ranges phenotypically from hyperuricaemia to Lesch-Nyhan... 
mutation | Lesch-Nyhan syndrome | HPRT | Lesch-Nyhan Syndrome | Mutation |