A new physiological medium uncovers biochemical and cellular alterations in Lesch-Nyhan disease fibroblasts
Paula Escudero-Ferruz,
Neus Ontiveros,
Claudia Cano-Estrada
et al.
Abstract:Background
Lesch-Nyhan disease (LND) is a severe neurological disorder caused by the genetic deficiency of hypoxanthine–guanine phosphoribosyltransferase (HGprt), an enzyme involved in the salvage synthesis of purines. To compensate this deficiency, there is an acceleration of the de novo purine biosynthetic pathway. Most studies have failed to find any consistent abnormalities of purine nucleotides in cultured cells obtained from the patients. Recently, it has been shown that 5-aminoimidazole-… Show more
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