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Biochemical Journal, ISSN 0264-6021, 04/2000, Volume 347, Issue 1, pp. 1 - 16
Journal Article
Hong Kong Journal of Paediatrics, ISSN 1013-9923, 07/2015, Volume 20, Issue 3, pp. 163 - 168
Objectives: To analyse the characteristics of mutation in PTS gene in Chinese patients with mild 6-pyruvoyl-tetrahydropterin synthase deficiency (M-PTSD).... 
Mutation | Medication treatment | Deficiency | Tetrahydropterin | 6-pyruvoyl-tetrahydropterin synthase deficiency | HYPERPHENYLALANINEMIA | Tetrahydropterin deficiency | PEDIATRICS | 6-PYRUVOYLTETRAHYDROPTERIN SYNTHASE | MUTATIONS
Journal Article
Journal Article
Journal Article
Coordination Chemistry Reviews, ISSN 0010-8545, 2011, Volume 255, Issue 9, pp. 1016 - 1038
Journal Article
Pathology, ISSN 0031-3025, 04/2019, Volume 51, Issue 3, pp. 274 - 280
Genetic defects on 6-pyruvoyl-tetrahydropterin synthase (PTPS) are the most prevalent cause of hyperphenylalaninaemia not due to phenylalanine hydrolyase... 
in silico prediction | OMIM, 261640 | PDB code, 3I2B | 3D protein structure | mutation analysis | POLYMORPHISMS | ENZYME | PTS GENE | MODEL | PATHOLOGY | BINDING SITE | 6-PYRUVOYL TETRAHYDROPTERIN SYNTHASE | MISSENSE MUTATIONS
Journal Article