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 plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6

27 Nov 2019

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 ATP Synthase and ATPases Research
Share to Drug-Induced Ocular Toxicity
Share to Mitochondrial Function and Pathology

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31776719
DOI: 10.1007/s00415-019-09619-z

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

Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6PMID 31776719Read ↗

Visual Recovery in Leber Hereditary Optic Neuropathy From a Rare mt.14568 Mutation on ND6 Gene.Semantic proximity Read ↗

Novel MT-ND5 gene mutation identified in Leber's hereditary optic neuropathy patient using mitochondrial genome sequencing.Semantic proximity Read ↗

Novel Mutations in the ND5 Gene Associated With Leber Hereditary Optic Neuropathy.Semantic proximity Read ↗

Leber's hereditary optic neuropathy plus dystonia caused by the mitochondrial ND1 gene m.4160 T > C mutation.Semantic proximity Read ↗

Leber's hereditary optic neuropathy: Update on the novel genes and therapeutic options.Semantic proximity Read ↗

An enigmatic pedigree of variable presentations of optic neuropathy due to mitochondrial-ND6 mutation.Semantic proximity Read ↗

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patientSemantic proximity Read ↗

Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635G > A and ND6 m.14502 T > C.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 case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation.Semantic proximity Read ↗

Painful vision loss in Leber hereditary optic neuropathy with novel ND1 variant mimicking optic neuritis.Semantic proximity Read ↗

Safety of rAAV2/2-ND4 Gene Therapy for Leber Hereditary Optic NeuropathySemantic proximity Read ↗

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