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pro vyhledávání: '"Nima Ebrahimpour Seraydar, M.D."'
Autor:
Akram Ehsasat Vatan, M.D., Amin Mottaghizade Gargari, M.D., Arian Haghtalab, M.D., Nima Ebrahimpour Seraydar, M.D.
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101173- (2024)
Objectives: Phenylketonuria is a hereditary condition caused by the deficiency of the enzyme phenylalanine hydroxylase, leading to abnormal phenylalanine metabolism. Managing phenylketonuria involves implementing dietary interventions to control phen
Externí odkaz:
https://doaj.org/article/de6a5163e5c747388f1df588d266c5cf
