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Phenylketonuria. The in vivo hydroxylation rate of phenylalanine into tyrosine is decreased.

In phenylketonuria (PKU), the enzyme phenylalanine hydroxylase is deficient, resulting in a decreased conversion of phenylalanine (Phe) into tyrosine (Tyr). The severity of the disease is expressed as the tolerance for Phe at 5 yr of age. In PKU patients it is assumed that the decreased conversion o...

詳細記述

保存先:
書誌詳細
主要な著者: van Spronsen, F J, Reijngoud, D J, Smit, G P, Nagel, G T, Stellaard, F, Berger, R, Heymans, H S
フォーマット: Artigo
言語:Inglês
出版事項: 1998
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC508879/
https://ncbi.nlm.nih.gov/pubmed/9637722
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