A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: relation of organic aciduria to phenotype?

doi:10.1007/BF01799643

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

Community

Back to search

Article

A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: relation of organic aciduria to phenotype?

Journal of inherited metabolic disease - 1 Jan 1992

Jakobs C, de Grauw A J

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 Abnormalities, Multiple
Share to Amino Acid Metabolism, Inborn Errors
Share to Ductus Arteriosus, Patent
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Source

Open in PubMed

Identifiers

PMID: 1527995
DOI: 10.1007/BF01799643

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 · 8 closest

A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: relation of organic aciduria to phenotype?PMID 1527995Read ↗

L-2-hydroxyglutaric aciduria: three Australian cases.Semantic proximity Read ↗

Pathogenesis of different clinical outcomes in spite of identical genotypes and comparable blood phenylalanine concentrations in phenylketonurics.Semantic proximity Read ↗

Human Metabolic Enzymes Deficiency: A Genetic Mutation Based ApproachSemantic proximity Read ↗

[Hereditary orotic aciduria].Semantic proximity Read ↗

Molecular basis for the phenotypical diversity of phenylketonuria and related hyperphenylalaninaemias.Semantic proximity Read ↗

Phenylketonuria - genetic, clinical and therapeutic aspectsSemantic proximity Read ↗

Human aldehyde dehydrogenases: potential pathological, pharmacological, and toxicological impact.Semantic proximity Read ↗

Primary aldosteronism: from genesis to genetics.Semantic proximity Read ↗

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