Associated Papers
Molybdenum cofactor deficiency: A natural history.
Spiegel R et al.
Journal of Inherited Metabolic Disease, 2022
A neonate with molybdenum cofactor deficiency type B.
Lin Y et al.
Translational Pediatrics, 2021
The Clinical and Molecular Characteristics of Molybdenum Cofactor Deficiency Due to MOCS2 Mutations.
Arican P et al.
Pediatric Neurology, 2019
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