Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assay.

Progress in clinical and biological research - 1 Jan 1990

Hale D E, Stanley C A, Coates P M

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acyl-CoA Dehydrogenase
Share to Acyl-CoA Dehydrogenase, Long-Chain
Share to Electron-Transferring Flavoproteins
Share to Fatty Acid Desaturases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fibroblasts

Share to Flavoproteins

Share to Leukocytes

Share to Substrate Specificity

Source

Identifiers

PMID: 2326298

Provenance

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

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assay.PMID 2326298Read ↗

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

Molecular analysis of medium-chain acyl-CoA dehydrogenase deficiency: a diagnostic approach.Semantic proximity Read ↗

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

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

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

Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death.Semantic proximity Read ↗

Multiple acyl-coenzyme A dehydrogenation disorders (MAD) responsive to riboflavin: biochemical studies in fibroblasts.Semantic proximity Read ↗

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of two new mutations.Semantic proximity Read ↗

Mutations of human medium-chian acyl-CoA dehydrogenase.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 ↗

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

Disease mechanisms and protein structures in fatty acid oxidation defects.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.