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

Reduced frequency of known mutations in a cohort of LHON patients from India.

Ophthalmic genetics - 1 Dec 2010

Sundaresan Periasamy, Kumar S Mahesh, Thompson Stewart, Fingert John H

Abstract excerpt

BACKGROUND: Three mitochondrial mutations account for 95% of Leber's hereditary optic neuropathy (LHON) in the European population: G3640A, G11778A and T14484C. The purpose of the study was to investigate the frequency of these mitochondrial DNA mutations in LHON patients from a South Indian popu...

Read the complete abstract on PubMed

Topics

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

Share to DNA, Mitochondrial
Share to DNA Mutational Analysis
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mitochondrial Diseases

Share to Optic Atrophy, Hereditary, Leber

Share to Sequence Analysis, DNA

Share to Young Adult

Source

Identifiers

PMID: 20809775
DOI: 10.3109/13816810.2010.510818

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20809775-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Reduced frequency of known mutations in a cohort of LHON patients from India.PMID 20809775Read ↗

Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.Semantic proximity Read ↗

Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.Semantic proximity Read ↗

A hospital-based five-year prospective study on the prevalence of Leber's hereditary optic neuropathy with genetic confirmation.Semantic proximity Read ↗

Prevalence of primary mutations in Leber hereditary optic neuropathy: A five-year report from a tertiary eye care center in India.Semantic proximity Read ↗

Mutation profile of neurodegenerative mitochondriopathy - LHON in Southern India.Semantic proximity Read ↗

Meta-analysis of the prevalence of Leber hereditary optic neuropathy mtDNA mutations in Europe.Semantic proximity Read ↗

The epidemiology and mutation types of Leber's hereditary optic neuropathy in Thailand.Semantic proximity Read ↗

Mitochondrial DNA variation of Leber’s Hereditary Optic Neuropathy (LHON) in Western SiberiaSemantic proximity Read ↗

Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR.Semantic proximity Read ↗

Leber's hereditary optic neuropathy with molecular characterization in two Indian families.Semantic proximity Read ↗

Mitochondrial DNA mutations in Korean patients with Leber's hereditary optic neuropathy.Semantic proximity Read ↗

Leber's hereditary optic neuropathy: clinical and molecular profile of a Brazilian sample.Semantic proximity Read ↗

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