Phenylketonuria as a model for protein misfolding diseases and for the development of next generation orphan drugs for patients with inborn errors of metabolism

Overview of attention for article published in Journal of Inherited Metabolic Disease, September 2010

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Chinese

苯丙氨酸羟化酶

Cited by user Htmlzycq on 28 Apr 2013

English

Phenylalanine hydroxylase

Cited by user Apeckwiki on 17 May 2011

Phenylalanine hydroxylase (PheOH, alternatively PheH or PAH) is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate…