(Q41226455)

28 September 2017

MGB probe assay for rapid detection of mtDNA11778 mutation in the Chinese LHON patients by real-time PCR. (English)

1 reference

28 September 2017

Jian-yong Wang

1

1 reference

28 September 2017

Yang-shun Gu

2

1 reference

28 September 2017

Jing Wang

3

1 reference

28 September 2017

Yi Tong

4

1 reference

28 September 2017

Ying Wang

5

1 reference

28 September 2017

Jun-bing Shao

6

1 reference

28 September 2017

Ming Qi

7

1 reference

28 September 2017

1 August 2008

1 reference

Journal of Zhejiang University. Science. B

28 September 2017

1 reference

28 September 2017

9

1 reference

28 September 2017

8

1 reference

28 September 2017

610-615

1 reference

Mitochondrion and its related disorders: making a comeback

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

LHON and other optic nerve atrophies: the mitochondrial connection

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

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

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Evaluation of minor groove binding probe and Taqman probe PCR assays: Influence of mismatches and template complexity on quantification

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Quantification of mitochondrial DNA deletion, depletion, and overreplication: application to diagnosis

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Quantitative analysis of human mitochondrial DNA using a real-time PCR assay

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

LHON (Leber's hereditary optic neuropathy)

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2491690

Genetic analysis in Leber's hereditary optic neuropathy using the comparative genomic hybridization technique

19 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18763310

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18763310

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18763310

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1631/JZUS.B0820058

1 reference

28 September 2017

1 reference

28 September 2017

PubMed publication ID

18763310

1 reference