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pro vyhledávání: '"Joud Alkhalifah"'
Autor:
Albandary AlBakheet, Hanan AlQudairy, Joud Alkhalifah, Sheikhah Almoaily, Namik Kaya, Zuhair Rahbeeni
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Background: Hypoxanthine-guanine phosphoribosyltransferase (HPRT1) deficiency is an inborn error of purine metabolism responsible for Lesch–Nyhan syndrome (LNS). The disease is inherited in an X-linked recessive manner and predominantly affects mal
Externí odkaz:
https://doaj.org/article/4e2c80f6c8d7492fb746d1f236332d6e
