Associated Papers
Molybdenum Cofactor Deficiency in Humans.
Johannes L et al.
Molecules (basel, Switzerland), 2022
Case Report: Compound Heterozygous Variants in MOCS3 Identified in a Chinese Infant With Molybdenum Cofactor Deficiency.
Tian Q et al.
Frontiers in Genetics, 2021
Editorial: Next Generation Sequencing (NGS) for Rare Diseases Diagnosis.
Yang XA
Frontiers in Genetics, 2021
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