Genetic testing for aldehyde dehydrogenase 2 deficiency in young adults.

doi:10.1038/tpj.2011.3

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

Genetic testing for aldehyde dehydrogenase 2 deficiency in young adults.

The pharmacogenomics journal - 1 Aug 2011

Hendershot C S

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 Alcohol Drinking
Share to Aldehyde Dehydrogenase
Share to Aldehyde Dehydrogenase, Mitochondrial
Share to California

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Privacy

Share to Metabolism, Inborn Errors

Share to Predictive Value of Tests

Share to Universities

Source

Open in PubMed Open full text

Identifiers

PMID: 21321583
DOI: 10.1038/tpj.2011.3
PMCID: PMC4120272

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

Genetic testing for aldehyde dehydrogenase 2 deficiency in young adults.PMID 21321583Read ↗

[Genetic testing and gene-based testing forAllergic disorders].Semantic proximity Read ↗

Genetic testing in asymptomatic minorsSemantic proximity Read ↗

Polymorphisms of Human Aldehyde DehydrogenasesSemantic proximity Read ↗

Genetic testing of children for late onset disease.Semantic proximity Read ↗

Molecular genetic testing for inherited disorders.Semantic proximity Read ↗

Molecular diagnosis of inborn errors of metabolism.Semantic proximity Read ↗

Rapid detection of ALDH2 genotypes by constant denaturant gel electrophoresis.Semantic proximity Read ↗

DNA diagnosis of hemoglobin mutations.Semantic proximity Read ↗

Testing for fragile X gene mutations throughout the life span.Semantic proximity Read ↗

Commentary: molecular analysis of congenital adrenal hyperplasia in a newborn screening program.Semantic proximity Read ↗

Aldehyde dehydrogenase 2 genotype in type 1 diabetes mellitus.Semantic proximity Read ↗

Genetic Testing for PheochromocytomaSemantic proximity Read ↗

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