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Article

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNA.

Journal of inherited metabolic disease - 1 Jan 1994

Andresen B S, Bross P, Knudsen I, Winter V, Kølvraa S, Bolund L, Gregersen N

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 7807932
DOI: 10.1007/BF00711806

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNA.PMID 7807932Read ↗

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Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene.Semantic proximity Read ↗

[Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency].Semantic proximity Read ↗

Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.Semantic proximity Read ↗

The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase gene.Semantic proximity Read ↗

Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: an update.Semantic proximity Read ↗

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspects.Semantic proximity Read ↗

Medium-chain acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiency.Semantic proximity Read ↗

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