Molybdenum Cofactor Deficiency (MoCD): Complementation Groups A–C
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1772-1
Reference17 articles.
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2. Duran M et al (1978) Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport? J Inherit Metab Dis 1:175–178. https://doi.org/10.1007/bf01805591
3. Johnson JL, Wuebbens MM, Mandell R, Shih VE (1989) Molybdenum cofactor biosynthesis in humans. Identification of two complementation groups of cofactor-deficient patients and preliminary characterization of a diffusible molybdopterin precursor. J Clin Invest 83:897–903. https://doi.org/10.1172/jci113974
4. Kang C (2021) Fosdenopterin: first approval. Drugs 81:953–956. https://doi.org/10.1007/s40265-021-01520-2
5. Kikuchi K, Hamano S, Mochizuki H, Ichida K, Ida H (2012) Molybdenum cofactor deficiency mimics cerebral palsy: differentiating factors for diagnosis. Pediatr Neurol 47:147–149. https://doi.org/10.1016/j.pediatrneurol.2012.04.013
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