The epidemiology of Leber hereditary optic neuropathy in the North East of England (Q24611047)

2

P G

Griffiths

1 reference

29 November 2023

D T Brown

3

D T

Brown

1 reference

29 November 2023

N Howell

4

N

Howell

1 reference

29 November 2023

D M Turnbull

5

D M

American Journal of Human Genetics

Turnbull

1 reference

29 November 2023

language of work or name

English

0 references

publication date

February 2003

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published in

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volume

72

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page(s)

333-9

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issue

2

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cites work

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees

1 reference

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A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

7 April 2017

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Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

7 April 2017

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

7 April 2017

1 reference

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Population frequencies of inherited neuromuscular diseases—A world survey

7 April 2017

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An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy

7 April 2017

1 reference

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Leber hereditary optic neuropathy

7 April 2017

1 reference

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Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

27 September 2017

1 reference

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Do idebenone and vitamin therapy shorten the time to achieve visual recovery in Leber hereditary optic neuropathy?

27 September 2017

2 references

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27 September 2017

https://api.crossref.org/works/10.1086%2F346066

7 January 2021

inferred from DOI database lookup

Multiplex fluorescence-based primer extension method for quantitative mutation analysis of mitochondrial DNA and its diagnostic application for Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

The incidence of thyroid disorders in the community: a twenty-year follow-up of the Whickham Survey

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

The epidemiology of Huntington's disease in Northern Ireland

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Leber hereditary optic neuropathy in Australia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

mtDNA mutations that cause optic neuropathy: how do we know?

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379226

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations

28 November 2018

1 reference

12 December 2020

De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy

1 reference

12 December 2020

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy

1 reference

12 December 2020

Human mitochondrial diseases: answering questions and questioning answers

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12 December 2020

The epidemiology of pathogenic mitochondrial DNA mutations

1 reference

12 December 2020

Prevalence of retinitis pigmentosa in Maine

1 reference

12 December 2020

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

1 reference

12 December 2020

Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation

1 reference

12 December 2020

Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation

1 reference

12 December 2020

Heteroplasmy in Leber's hereditary optic neuropathy

1 reference

12 December 2020

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

12 December 2020

Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects

1 reference

12 December 2020

Identifiers

DOI

10.1086/346066

1 reference

3023591

3023591

1 reference

1 reference

1 reference