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

Topics Community

Article

Human gene mutations. Gene symbol: AR. Disease: Androgen insensitivity syndrome.

Human genetics - 1 Jan 2004

Jung S C, Lee K S, Koo S K

Abstract excerpt

No abstract is available from the source.

Topics

Androgen-Insensitivity Syndrome
Humans
Male
Mutation
Receptors, Androgen

Source

Identifiers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

PMID

15046097

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Human gene mutations. Gene symbol: AR. Disease: Androgen insensitivity syndrome.PMID 15046097Read ↗

Novel human pathological mutations. Gene symbol: AR. Disease: androgen insensitivity syndrome.Semantic proximity Read ↗

[Androgen receptor mutation].Semantic proximity Read ↗

Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.Semantic proximity Read ↗

Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center CohortSemantic proximity Read ↗

Molecular biology of androgen insensitivity.Semantic proximity Read ↗

[Androgen insensitivity syndrome].Semantic proximity Read ↗

Androgen receptor defects: historical, clinical, and molecular perspectives.Semantic proximity Read ↗

The androgen receptor gene mutations database.Semantic proximity Read ↗

Human androgen insensitivity syndrome.Semantic proximity Read ↗

Androgen insensitivity syndrome: clinical features and molecular defects.Semantic proximity Read ↗

Human gene mutations. Gene symbol: CYP19. Disease: Aromatase deficiency.Semantic proximity Read ↗

Genetic Findings in a Cohort of Patients with Androgen Insensitivity SyndromeSemantic proximity Read ↗

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