Potential molecular link between the β-amyloid precursor protein (APP) and hypoxanthine-guanine phosphoribosyltransferase (HGprt) enzyme in Lesch-Nyhan disease and cancer

Lesch-Nyhan disease (LND) is a rare X-linked inherited neurogenetic disorders of purine metabolic in which the cytoplasmic enzyme, hypoxanthine-guanine phosphoribosyltransferase (HGprt) is defective. Despite having been characterized over 60 years ago, however, up to now, there is no satisfactory ex...

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Autor principal: Khue Vu Nguyen
Formato: article
Lenguaje:EN
Publicado: AIMS Press 2021
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Acceso en línea:https://doaj.org/article/87a45eae98444dcf8a8626b01e50e7e2
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