The Clinical Aspects of HGPRT Deficiency

Autor: I. Kamilli, U. Gresser
Rok vydání: 1993
Předmět:
Zdroj: Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism ISBN: 9783642849640
DOI: 10.1007/978-3-642-84962-6_2
Popis: The enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT) catalyzes in the presence of 5-phosphoribosyl-1-pyrophosphate (PRPP) the formation of inosine-5-monophosphate and guanosine monophosphate from the bases hypoxanthine and guanine.
Databáze: OpenAIRE