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

LOXL1 Mutations Are Associated with Exfoliation Syndrome in Patients from the Midwestern United States

26 Nov 2007

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 Atherosclerosis and Cardiovascular Diseases
Share to Cell Adhesion Molecules Research
Share to Glaucoma and retinal disorders

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18036875
DOI: 10.1016/j.ajo.2007.09.034

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

LOXL1 Mutations Are Associated with Exfoliation Syndrome in Patients from the Midwestern United StatesPMID 18036875Read ↗

Association Between LOXL1 and pseudoexfoliation.Semantic proximity Read ↗

The role of lysyl oxidase-like 1 (LOXL1) in exfoliation syndrome and glaucomaSemantic proximity Read ↗

Major review: Exfoliation syndrome; advances in disease genetics, molecular biology, and epidemiologySemantic proximity Read ↗

LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome.Semantic proximity Read ↗

Association of lysyl oxidase-like 1 gene polymorphisms with exfoliation syndrome in Koreans.Semantic proximity Read ↗

Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.Semantic proximity Read ↗

Systemic diseases associated with exfoliation syndrome.Semantic proximity Read ↗

Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report.Semantic proximity Read ↗

Exfoliation syndrome: prevalence and inheritance in a subisolate of the Finnish populationSemantic proximity Read ↗

Evaluation of LOXL1 polymorphisms in exfoliation syndrome in a Chinese population.Semantic proximity Read ↗

Genetics of Exfoliation SyndromeSemantic proximity Read ↗

LOXL1 gene polymorphisms are associated with exfoliation syndrome/exfoliation glaucoma risk: An updated meta-analysis.Semantic proximity Read ↗

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