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Article

Molybdenum Cofactor Deficiency in the Neonate: Expanding the Phenotype.

Pediatric neurology - 1 Apr 2024

Hierro Fátima, Tomé Maria Luís, Grenha Joana, Santos Helena, Santos Fátima, Nunes Joana

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 38367485
DOI: 10.1016/j.pediatrneurol.2024.01.020

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Molybdenum Cofactor Deficiency in the Neonate: Expanding the Phenotype.PMID 38367485Read ↗

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