Cite
HARVARD Citation
Huijmans, J. et al. (2017). Molybdenum cofactor deficiency: Identification of a patient with homozygote mutation in the MOCS3 gene. American journal of medical genetics. 173 (6), pp. 1601-1606. [Online].
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Huijmans, J. et al. (2017). Molybdenum cofactor deficiency: Identification of a patient with homozygote mutation in the MOCS3 gene. American journal of medical genetics. 173 (6), pp. 1601-1606. [Online].