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Article

Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.

Journal of inherited metabolic disease - 1 Jan 2003

Treacy E P, Lee-Chong A, Roche G, Lynch B, Ryan S, Goodman S

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Share to Amino Acid Metabolism, Inborn Errors
Share to Diet, Protein-Restricted
Share to Glutarates
Share to Glutaryl-CoA Dehydrogenase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 12872844
DOI: 10.1023/a:1024087832406

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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