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

Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

Progress in clinical and biological research - 1 Jan 1992

Matsubara Y, Narisawa K, Tada K, Ikeda H, Yeqi Y, Danks D M, Green A, McCabe E R

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 Dehydrogenases
Share to Blood Stains
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Metabolism, Inborn Errors

Share to Polymorphism, Restriction Fragment Length

Share to Prevalence

Source

Identifiers

PMID: 1359564

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.PMID 1359564Read ↗

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 ↗

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.Semantic proximity Read ↗

Is genotyping useful for the screening of medium-chain acyl-CoA dehydrogenase deficiency in France?Semantic proximity Read ↗

Rapid, comprehensive screening of the human medium chain acyl-CoA dehydrogenase geneSemantic proximity Read ↗

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

Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Late-onset multiple acyl-CoA dehydrogenase deficiency: a frequently missed diagnosis?Semantic proximity Read ↗

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

A985G mutation incidence in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Brazil.Semantic proximity Read ↗

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

Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspective.Semantic proximity Read ↗

Prevalence of the 985A>G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Sweden.Semantic proximity Read ↗

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