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pro vyhledávání: '"Nikola Anna Intlere"'
Autor:
Iveta Abola, Nikola Anna Intlere, Anda Brinkmane, Sabine Laktina, Agnese Zarina, Lauma Vasilevska, Ingus Skadins, Georgijs Moisejevs, Linda Gailite, Madara Auzenbaha
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101167- (2024)
Background: Phenylketonuria (PKU) is an autosomal recessive inherited disorder of phenylalanine (Phe) metabolism that results from a deficiency of phenylalanine hydroxylase (PAH). Patients with PKU rely on amino acid mixtures and low-protein diets, w
Externí odkaz:
https://doaj.org/article/accda48c629a4bfdb47dd9c5242da498
