Leber's hereditary optic neuropathy with spontaneous recovery;Lebersche optikusneuropathie mit klinischer besserung

Ophthalmologe

Volumn 97, Issue 12, 2000, Pages 849-854

  Leo Kottler, B ^a   Jacobi, F ^a   Christ Adler, M ^a  

^a Abteilung II: Pathophysiologie des Sehens und Neuroophthalmologie   (Germany)

Author keywords

Leber hereditary optic neuropathy; Mitochondrial DNA; mtDNA; Point mutation; Spontaneous recovery

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; DISEASE COURSE; GENETIC DISORDER; HUMAN; LEBER CONGENITAL AMAUROSIS; OPHTHALMOSCOPY; PEDIGREE; VISUAL ACUITY;

EID: 0034480542     PISSN: 0941293X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003470070007     Document Type: Article

References (24)

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2. Leber's hereditary optic neuropathy: Clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene
3. Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia
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5. Primary LHON mutations: Trying to separate"fruyt"from"chaf"
6. Leber hereditary optic neuropathy: Respiratory chain dysfunction and degeneration of the optic nerve
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10. A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia
11. A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidase phosphorylation in a family with Leber hereditary optic neuropathy
12. Ueber hereditäre und congenital-angelegte sehnervenleiden
13. Korrelation klinischer und molekulargenetischer befunde bei Leberscher optikusneuropathie
14. Leber's hereditary optic neuropathy: Clinical and molecular genetic results obtained in a family with a new point mutation at nulcleotide position 14498 in the ND6 gene
15. Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON)
16. A simple salting out procedure for extracting DNA from human nucleated cells
17. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
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19. Leber's hereditary optic neuropathy: Correlations between mitochondrial genotype and visual outcome
20. The clinical features of Leber hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
21. Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation
22. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
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24. Mitochondrial DNA mutation in Leber's hereditary optic neuropathy