(Q44086295)

29 November 2017

title

The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees (English)

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Leber hereditary optic neuropathy

29 November 2017

main subject

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4

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29 November 2017

author name string

Nopasak Phasukkijwatana

1

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29 November 2017

Wanicha L Chuenkongkaew

2

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29 November 2017

Rungnapa Suphavilai

3

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29 November 2017

Sarinee Pingsuthiwong

5

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29 November 2017

Ngamkae Ruangvaravate

6

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29 November 2017

La-ongsri Atchaneeyasakul

7

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29 November 2017

Sukhuma Warrasak

8

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29 November 2017

Anuchit Poonyathalang

9

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29 November 2017

Thanyachai Sura

10

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29 November 2017

Patcharee Lertrit

11

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29 November 2017

publication date

14 February 2006

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Journal of Human Genetics

29 November 2017

published in

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29 November 2017

volume

51

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29 November 2017

issue

4

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29 November 2017

page(s)

298-304

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https://scigraph.springernature.com/pub.10.1007/s10038-006-0361-1

29 November 2017

exact match

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cites work

Leber's hereditary optic neuropathy. New genetic considerations

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-006-0361-1

mtDNA mutations in Leber's hereditary optic neuropathy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-006-0361-1

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

21 January 2018

1 reference

12 December 2020

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

1 reference

12 December 2020

Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation

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12 December 2020

Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy

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12 December 2020

A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus

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12 December 2020

Leber hereditary optic neuropathy: how do mitochondrial DNA mutations cause degeneration of the optic nerve?

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12 December 2020

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

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12 December 2020

Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA

1 reference

12 December 2020

A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy

1 reference

12 December 2020

The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle

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12 December 2020

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

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12 December 2020

An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy

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12 December 2020

Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy

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12 December 2020

Leber's hereditary optic neuropathy--the spectrum of mitochondrial DNA mutations in Chinese patients

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12 December 2020

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

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12 December 2020

Leber's hereditary optic neuropathy in Thailand

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12 December 2020

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

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12 December 2020

Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve

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12 December 2020

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

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12 December 2020

The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy

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12 December 2020

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

1 reference

12 December 2020

Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease

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12 December 2020

Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations

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12 December 2020

Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction

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12 December 2020

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees

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12 December 2020

Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy

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12 December 2020

Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation

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12 December 2020

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

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12 December 2020

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

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12 December 2020

'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation

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12 December 2020

Heteroplasmy in Leber's hereditary optic neuropathy

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12 December 2020

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

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12 December 2020

Suppression of complex I gene expression induces optic neuropathy

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12 December 2020

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

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12 December 2020

Evaluation of the importance of maternal history of diabetes and of mitochondrial variation in the development of NIDDM.

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12 December 2020

Leber hereditary optic neuropathy

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12 December 2020

10.1007/S10038-006-0361-1

Identifiers

DOI

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29 November 2017

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