Associated Papers
Novel pathogenic variant in a mild case of type B molybdenum cofactor deficiency: case report and literature review.
Kinsinger M et al.
Bmc Medical Genomics, 2024
39695700 (PubMed )
Supplement: 12920_2024_2027_MOESM1_ESM.zip › Supplementary › Supplementary_Online_Only_Table_1_MOCS2_6.2.24.xlsx › all_cases
Molybdenum Cofactor Deficiency in Humans.
Johannes L et al.
Molecules (basel, Switzerland), 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
Critical appraisal of genotype assessment in molybdenum cofactor deficiency.
Hinderhofer K et al.
Journal of Inherited Metabolic Disease, 2017
Investigation of molybdenum cofactor deficiency due to MOCS2 deficiency in a newborn baby.
Edwards M et al.
Meta Gene, 2015
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