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

Mitochondrial sequence changes in keratoconus patients.

Investigative ophthalmology & visual science - 20 Mar 2014

Abu-Amero Khaled K, Azad Taif Anwar, Kalantan Hatem, Sultan Tahira, Al-Muammar Abdulrahman M

Abstract excerpt

PURPOSE: We investigated whether a group of patients with keratoconus (KTCN) harbor mutations in the mitochondrial genome. METHODS: We sequenced the full mitochondrial genome in a group of Saudi patients with KTCN (n = 26) and 100 ethnically matched controls who had no KTCN by examination. RESULT...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Corneal surgery and disorders
Share to DNA, Mitochondrial
Share to Genome, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glaucoma and retinal disorders

Share to Keratoconus

Share to Mitochondria

Share to Mutation

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 24569587
DOI: 10.1167/iovs.14-13938

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24569587-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mitochondrial sequence changes in keratoconus patients.PMID 24569587Read ↗

Association of mitochondrial haplogroups H and R with keratoconus in Saudi Arabian patients.Semantic proximity Read ↗

Whole mitochondrial genome analysis in Chinese patients with keratoconus.Semantic proximity Read ↗

Mitochondrial complex 1 gene analysis in keratoconus.Semantic proximity Read ↗

Decreased Integrity, Content, and Increased Transcript Level of Mitochondrial DNA Are Associated with KeratoconusSemantic proximity Read ↗

Mitochondrial DNA copy number, but not haplogroup is associated with keratoconus in Han Chinese population.Semantic proximity Read ↗

Mitochondrial DNA nucleotide changes in primary congenital glaucoma patients.Semantic proximity Read ↗

Mitochondrial sequence variation in African-American primary open-angle glaucoma patients.Semantic proximity Read ↗

Mitochondrial dysfunction and oxidative stress in corneal diseaseSemantic proximity Read ↗

Massively parallel sequencing of mitochondrial genome in primary open angle glaucoma identifies somatically acquired mitochondrial mutations in ocular tissue.Semantic proximity Read ↗

Role of mitochondrial dysfunction in ocular surface diseasesSemantic proximity Read ↗

Analysis of mitochondrial DNA variations in Indian patients with congenital cataract.Semantic proximity Read ↗

Mitochondrial transfer RNA variants and primary congenital glaucoma.Semantic proximity Read ↗

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