(Q33728325)

28 July 2017

title

Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C (English)

1 reference

28 July 2017

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Yong-Gang Yao

7

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author name string

Dandan Yu

1

1 reference

28 July 2017

Xiaoyun Jia

2

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28 July 2017

A-Mei Zhang

3

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28 July 2017

Shiqiang Li

4

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28 July 2017

Yang Zou

5

1 reference

28 July 2017

Qingjiong Zhang

6

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28 July 2017

language of work or name

English

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publication date

18 October 2010

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28 July 2017

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28 July 2017

volume

5

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28 July 2017

issue

10

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28 July 2017

page(s)

e13426

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Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

18 October 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity

21 June 2018

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Gene-environment interactions in Leber hereditary optic neuropathy

21 June 2018

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Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation

21 June 2018

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Inherited mitochondrial optic neuropathies

21 June 2018

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Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

21 June 2018

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Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.

21 June 2018

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Pseudomitochondrial genome haunts disease studies.

21 June 2018

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Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

21 June 2018

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Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.

21 June 2018

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Mitochondrial DNA sequence variation in single cells from leukemia patients

21 June 2018

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Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics

21 June 2018

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Leber's hereditary optic neuropathy: a multifactorial disease.

21 June 2018

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Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

21 June 2018

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Mitochondrial dysfunction as a cause of optic neuropathies

21 June 2018

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Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences

21 June 2018

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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

21 June 2018

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Reconstructing the evolutionary history of China: a caveat about inferences drawn from ancient DNA

21 June 2018

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Leber hereditary optic neuropathy

21 June 2018

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Phylogeographic differentiation of mitochondrial DNA in Han Chinese

21 June 2018

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Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families

21 June 2018

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Mitochondrial DNA polymorphisms in bipolar disorder

21 June 2018

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

21 June 2018

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 June 2018

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

21 June 2018

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2956641

A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2956641

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

21 June 2018

1 reference

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Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.

21 June 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Cytochrome b mutations in Leber hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Novel mitochondrial DNA mutations associated with Chinese familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

mtDNA tree Build 17 (18 Feb 2016)

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0013426

Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy

21 January 2018

1 reference

12 December 2020

Cytochrome c oxidase mutations in Leber hereditary optic neuropathy

1 reference

12 December 2020

Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A

1 reference

12 December 2020

The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0013426

Identifiers

DOI

1 reference

28 July 2017

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28 July 2017

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