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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
Autor:
Keskin, Fatma Nur1, Şahin, Teslime Özge1, Capasso, Raffaele2, Ağagündüz, Duygu1 duyguturkozu@gazi.edu.tr
Publikováno v:
Clinical & Experimental Pediatrics. Aug2023, Vol. 66 Issue 8, p320-331. 12p.
Handbook of Sourdough Microbiota and Fermentation: Food Safety, Health Benefits, and Product Development links the cereal and sourdough-based microorganisms, fermentations and microbial metabolites with food hygiene and safety, functional and health