Mitochondrial DNA abnormalities in ophthalmological disease. - Wikidata - awgldk - TriplyDB

Mitochondrial DNA abnormalities in ophthalmological disease.

Mitochondrial DNA abnormalities in ophthalmological disease.

http://www.wikidata.org/entity/Q37060104

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The Eye on Mitochondrial Disorders.Thiamine deficiency induces oxidative stress in brain mitochondria of Mus musculus.

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Mitochondrial DNA abnormalities in ophthalmological disease.

http://www.wikidata.org/entity/Q37060104

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

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scientific article published on 18 February 2011

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vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

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name

Mitochondrial DNA abnormalities in ophthalmological disease.

@en

Mitochondrial DNA abnormalities in ophthalmological disease.

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type

label

Mitochondrial DNA abnormalities in ophthalmological disease.

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Mitochondrial DNA abnormalities in ophthalmological disease.

@nl

prefLabel

Mitochondrial DNA abnormalities in ophthalmological disease.

@en

Mitochondrial DNA abnormalities in ophthalmological disease.

@nl

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J.SJOPT.2011.02.002

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Saudi journal of ophthalmology

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Mitochondrial DNA abnormalities in ophthalmological disease.

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Robert W Taylor

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Role of adenine nucleotide translocator 1 in mtDNA maintenance

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia

The epidemiology of Leber hereditary optic neuropathy in the North East of England

Mitochondrial DNA mutations in human disease

Retinopathy of NARP syndrome

Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome

A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation.

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395-404

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scholarly article

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10.1016/J.SJOPT.2011.02.002

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Gráinne S. Gorman

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2011-02-18T00:00:00Z

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mitochondrial DNA

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