(Q48706853)

14 February 2018

title

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. (English)

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14 February 2018

hereditary optic neuropathy

main subject

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N J Newman

1

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14 February 2018

M T Lott

series ordinal

2

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14 February 2018

D C Wallace

series ordinal

3

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14 February 2018

language of work or name

English

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publication date

1 June 1991

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14 February 2018

American Journal of Ophthalmology

published in

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14 February 2018

volume

111

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14 February 2018

page(s)

750-762

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14 February 2018

issue

6

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14 February 2018

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Variable genotype of Leber's hereditary optic neuropathy patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Prevalence and predictors of rhabdomyolysis in patients with hypokalemia

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

The molecular genetics of Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Mitochondria and Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

The early phase in Leber hereditary optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Fundus findings in Leber's hereditary optic neuroretinopathy. III. Fluorescein angiographic studies

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Ocular Fundus in Acute Leber Optic Neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

LEBER'S DISEASE IN THE NETHERLANDS.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

1 reference

7 January 2021

The inheritance of Leber's disease. A genealogical follow-up study

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Leber's optic neuropathy: a clinical and visual evoked potential study of affected and asymptomatic members of a six generation family

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Bilateral optic neuropathy with remission in young men. Variation on a theme by Leber?

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. I. Fundus findings in asymptomatic family members

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Leber's disease and dystonia: a mitochondrial disease

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Neurological studies in families with Leber's optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

The heart in Leber's optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Magnetic resonance imaging in Leber's optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Leber's optic neuropathy: clinical and visual evoked response studies in asymptomatic and symptomatic members of a 4-generation family

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976784-4

7 January 2021

10.1016/S0002-9394(14)76784-4

Identifiers

DOI

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PubMed ID

2039048

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14 February 2018