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Allosteric Guideline of Phenylalanine Hydroxylase
Short Communication: J Obes Metab 2024, 7:217
DOI: 10.4172/jomb.1000217
Ampleness of Nitisinone for the Administration of Alkaptonuria
Commentary: J Obes Metab 2024, 7:218
DOI: 10.4172/jomb.1000218
Conformational Adaptability in Phenylalanine Hydroxylase
Expert Review: J Obes Metab 2024, 7:219
DOI: 10.4172/jomb.1000219
Electrophoresis-Based PAH Genotyping in Chinese Han Population
Rapid Communication: J Obes Metab 2024, 7:221
DOI: 10.4172/jomb.1000221
Investigating Phenylalanine/Tyrosine Pathway Fluctuations in Alkaptonuria under Nitisinone Treatment
Perspective: J Obes Metab 2024, 7:222
DOI: 10.4172/jomb.1000222
Phenylalanine Diet in Infants with PAH Deficiency: Sapropterin Monotherapy Consideration
Mini Review: J Obes Metab 2024, 7:223
DOI: 10.4172/jomb.1000223
Thermodynamics of PAH with Iron, Tetrahydrobiopterin, and Phenylalanine
Short Communication: J Obes Metab 2024, 7:224
DOI: 10.4172/jomb.1000224
Utilization of Hematin in Tyrosinemia Type I
Mini Review: J Obes Metab 2024, 7:225
DOI: 10.4172/jomb.1000225
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