Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Fatma Nur, Keskin"'
Publikováno v:
Clinical and Experimental Pediatrics, Vol 66, Iss 8, Pp 320-331 (2023)
Phenylketonuria (PKU), an autosomal recessive inherited metabolic disorder, is caused by a mutation in the phenylalanine hydroxylase (PAH) gene on the 12th chromosome. Defective PAH activity ultimately leads to increased phenylalanine (Phe) blood con
Externí odkaz:
https://doaj.org/article/ec1c351bb9644a9ebef76c462daa8c0e
Publikováno v:
Clinical and Experimental Pediatrics.
Phenylketonuria (PKU), an autosomal recessive inherited metabolic disorder, is caused by a mutation in the phenylalanine hydroxylase (PAH) gene on the 12th chromosome. Defective PAH activity ultimately leads to increased phenylalanine (Phe) blood con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7167f2084cc0cb703bd2a07e5808fce4
https://doi.org/10.3345/cep.2022.00584
https://doi.org/10.3345/cep.2022.00584