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Phenylketonuria (PKU) is an autosomal recessive inborn error of metabolism (IEM) caused by mutations in the phenylalanine hydroxylase (PAH) gene. The molecular mechanism underlying deficiency of the PAH protein is, in mo...
Molecular mechanisms of PAH function in response to phenylalanine and tetrahydrobiopterin binding is an episode from Fakultät für Chemie und Pharmazie - Digitale Hochschulschriften der LMU - Teil 06/06 by Ludwig-Maximilians-Universität Münc...
This episode belongs to Fakultät für Chemie und Pharmazie - Digitale Hochschulschriften der LMU - Teil 06/06.
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Published Mar 17, 2016, 0 long, audio available.