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

Trimethylaminuria (fish malodour syndrome): a "benign" genetic condition with major psychosocial sequelae.

The Medical journal of Australia - 20 Oct 2008

Mountain Helen, Brisbane Joanna M, Hooper Amanda J, Burnett John R, Goldblatt Jack

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 Fishes
Share to Methylamines
Share to Mutation
Share to Odorants

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Oxygenases

Share to Syndrome

Source

Identifiers

PMID: 18928446
DOI: 10.5694/j.1326-5377.2008.tb02126.x

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

Trimethylaminuria (fish malodour syndrome): a "benign" genetic condition with major psychosocial sequelae.PMID 18928446Read ↗

Fish Malodour syndrome in a child.Semantic proximity Read ↗

Primary trimethylaminuria (fish odor syndrome) and hypothyroidism in an adolescent.Semantic proximity Read ↗

Trimethylaminuria (fish-odor syndrome): a case report.Semantic proximity Read ↗

Trimethylaminuria (fish odor syndrome): genotype characterization among Portuguese patients.Semantic proximity Read ↗

Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome.Semantic proximity Read ↗

Clinical utility gene card for: Trimethylaminuria - update 2014.Semantic proximity Read ↗

Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.Semantic proximity Read ↗

Trimethylaminuria.Semantic proximity Read ↗

Clinical utility gene card for: trimethylaminuria.Semantic proximity Read ↗

A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene.Semantic proximity Read ↗

Biochemical and clinical aspects of the human flavin-containing monooxygenase form 3 (FMO3) related to trimethylaminuria.Semantic proximity Read ↗

[Trimethylaminuria].Semantic proximity Read ↗

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