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Publikováno v:
Pharmaceuticals, Vol 17, Iss 1, p 31 (2023)
Erythropoietic protoporphyria (EPP) is a genetic disorder stemming from reduced ferrochelatase expression, the final enzyme in the pathway of heme biosynthesis. A closely related condition, X-linked protoporphyria (XLP), bears similar clinical featur
Externí odkaz:
https://doaj.org/article/b27547bc45c64dba972240cb304b0998