Plasma phospholipidome analysis reveals a different profile between children with phenylketonuria and healthy children
Phenylketonuria (PKU) is the most prevalent innate error in amino acid metabolism. PKU is characterized by the deficiency of a phenylalanine (Phe) metabolism enzyme, phenylalanine hydroxylase, which is responsible for the conversion of Phe into tyrosine (Tyr). Deficiency of this enzyme causes the ac...
| Autor principal: | |
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| Formato: | masterThesis |
| Idioma: | eng |
| Publicado em: |
2022
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| Texto completo: | http://hdl.handle.net/10773/30612 |
| País: | Portugal |
| Oai: | oai:ria.ua.pt:10773/30612 |