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

Leber hereditary optic neuropathy harboring a rare m.12811 T>C mitochondrial DNA mutation.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie - 1 Jun 2021

Zhou Han Peng, Ishikawa Hitoshi, Yasumoto Ryoma, Sakurai Keizo, Sawamura Hiromasa

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 DNA, Mitochondrial
Share to Mitochondria
Share to Mutation
Share to Optic Atrophy, Hereditary, Leber

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33493461
DOI: 10.1016/j.jcjo.2020.12.022

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Leber hereditary optic neuropathy harboring a rare m.12811 T>C mitochondrial DNA mutation.PMID 33493461Read ↗

Variable Presentation of Leber Hereditary Optic Neuropathy in Children of a Family Harboring a Rare m.13051G>A mtDNA Mutation.Semantic proximity Read ↗

Mitochondrial DNA mutation 14487T>C manifesting as Leber's hereditary optic neuropathy.Semantic proximity Read ↗

Leber Hereditary Optic Neuropathy in a Mother and Daughter Associated With m.10197G>A Mutation.Semantic proximity Read ↗

Novel Mutations of mtDNA m.14568G>A/m.14568C>T in MT-ND6 and m.7299A>G in MT-CO1: Evidence of Pathogenicity in Leber Hereditary Optic Neuropathy.Semantic proximity Read ↗

A Novel Mitochondrial Mutation for Lebers Hereditary Optic Neuropathy Presenting With Vitamin B12 Deficiency.Semantic proximity Read ↗

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

Leber hereditary optic neuropathy-new insights and old challenges.Semantic proximity Read ↗

[Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber's hereditary optic neuropathy].Semantic proximity Read ↗

[Study on three common mitochondrial DNA mutations in Leber's hereditary optic neuropathy].Semantic proximity Read ↗

Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation.Semantic proximity Read ↗

Mitochondrial DNA variants in a cohort from Argentina with suspected Leber's hereditary optic neuropathy (LHON).Semantic proximity Read ↗

m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.Semantic proximity Read ↗

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