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Article

CUGC for hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.

European journal of human genetics : EJHG - 1 Jul 2020

Martinelli Diego, Fiermonte Giuseppe, Häberle Johannes, Boenzi Sara, Goffredo Bianca Maria, Travaglini Lorena, Agolini Emanuele, Porcelli Vito, Dionisi-Vici Carlo

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Share to Genetic Testing
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Share to Mitochondrial Membrane Transport Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Ornithine

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Identifiers

PMID: 32242103
DOI: 10.1038/s41431-020-0616-x
PMCID: PMC7316770

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