(Q82444011)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population (English)

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

Leber hereditary optic neuropathy

26 August 2024

main subject

1 reference

5

Qingjiong Zhang

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074518

26 August 2024

author name string

Xiaoyun Jia

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Shiqiang Li

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Panfeng Wang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Xiangming Guo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074518

26 August 2024

publication date

11 November 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

16 January 2020

https://api.elsevier.com/content/article/PII:S0006291X10020656?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

https://api.elsevier.com/content/article/PII:S0006291X10020656?httpAccept=text/plain

26 August 2024

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

Biochemical and Biophysical Research Communications

26 August 2024

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

403

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

page(s)

237-241

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

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

16 January 2020

cites work

1 reference

7 July 2024

https://opencitations.net/index/api/v1/citations/10.1086/519394

Inherited mitochondrial optic neuropathies

1

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

26 August 2024

2

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families

26 August 2024

4

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

5

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

6

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

mtDNA haplogroup distribution in Chinese patients with Leber’s hereditary optic neuropathy and G11778A mutation

26 August 2024

7

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

8

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

9

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

10

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

11

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese

26 August 2024

12

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

13

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

No association between the SNPs (rs3749446 and rs1402000) in the PARL gene and LHON in Chinese patients with m.11778G>A

26 August 2024

14

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

15

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

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

26 August 2024

16

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

Sequence variation in mitochondrial complex I genes: mutation or polymorphism?

26 August 2024

18

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.11.017

26 August 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21074518%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference