NEOPTERIN DEFICIENCY: A CAUSE FOR HYPERPHENYLALANINEMIA
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Autosomal Recessive Guanosine Triphosphate Cyclohydrolase I Deficiency: Redefining the Phenotypic Spectrum and Outcomes;Movement Disorders Clinical Practice;2024-07-12
2. Characterization of Mouse and Human GTP Cyclohydrolase I Genes;Journal of Biological Chemistry;1995-04
3. A missense mutation in a patient with guanosine triphosphate cyclohydrolase I deficiency missed in the newborn screening program;The Journal of Pediatrics;1995-03
4. Hyperphenylalaninemia Due to Inherited Deficiencies of Tetrahydrobiopterin;Advances in Pediatrics;1989
5. Phenylketonuria and Hyperphenylalaninemia;Neurocutaneous Diseases;1987
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