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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Nov 3, 2024. (Total: 233167Documents)
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Query Trace: Molybdenum Cofactor Deficiency[original query]
The Clinical and Molecular Characteristics of Molybdenum Cofactor Deficiency Due to MOCS2 Mutations.
Pediatric neurology 2019 6 99 55-59.
Arican Pinar, Gencpinar Pinar, Kirbiyik Ozgur, Bozkaya Yilmaz Sema, Ersen Atilla, Oztekin Ozgur, Olgac Dundar Nih
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