In silico screening and molecular dynamics simulation of deleterious PAH mutations responsible for phenylketonuria genetic disorder
Author:
Affiliation:
1. Department of Chemistry University of Illinois at Chicago Chicago Illinois USA
Publisher
Wiley
Subject
Molecular Biology,Biochemistry,Structural Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/prot.26051
Reference62 articles.
1. Phenylalanine hydroxylase deficiency
2. Phenylketonuria
3. Phenylketonuria: a new look at an old topic, advances in laboratory diagnosis, and therapeutic strategies;Sumaily K;Int J Health Sci,2017
4. New Strategies for the Treatment of Phenylketonuria (PKU)
5. Structure of full-length human phenylalanine hydroxylase in complex with tetrahydrobiopterin
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