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

[Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease].

Duodecim; laaketieteellinen aikakauskirja - 1 Jan 1994

Sipilä I, Valle D, Mitchell G A, Brody L C

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 Blindness
Share to Finland
Share to Metabolism, Inborn Errors
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ornithine

Source

Identifiers

PMID: 8542823

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease].PMID 8542823Read ↗

Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophy.Semantic proximity Read ↗

[Gene errors in muscular diseases].Semantic proximity Read ↗

[Hyperuricemia associated with inborn errors of purine metabolism: screening, enzymatic and genetic diagnosis].Semantic proximity Read ↗

[Hereditary orotic aciduria].Semantic proximity Read ↗

[DNA instability and neurological diseases: a new model for genetic disease].Semantic proximity Read ↗

First report of c.425-1G>A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia.Semantic proximity Read ↗

Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspects.Semantic proximity Read ↗

[Mitochondrial ornithine transporter deficiency].Semantic proximity Read ↗

Hyperornithinaemia- hyperammonaemia- homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporterSemantic proximity Read ↗

[Complex I deficiency due to mutations in nuclear-encoded subunit genes].Semantic proximity Read ↗

[Inborn error of amino acids metabolism--general aspect].Semantic proximity Read ↗

Current Insight into Human Ornithine Aminotransferase: A Review.Semantic proximity Read ↗

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