Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population (Q73841466)

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7 November 2019

title

Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339587%20AND%20SRC:MED&resulttype=core&format=json

hereditary optic neuropathy

7 November 2019

main subject

1 reference

Dogulu CF

1

1 reference

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7 November 2019

Kansu T

2

1 reference

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7 November 2019

Seyrantepe V

3

1 reference

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7 November 2019

Ozguc M

4

1 reference

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7 November 2019

Topaloglu H

5

1 reference

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7 November 2019

Johns DR

6

1 reference

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7 November 2019

publication date

1 April 2001

1 reference

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7 November 2019

1 reference

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7 November 2019

volume

15

1 reference

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7 November 2019

issue

Pt 2

1 reference

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7 November 2019

page(s)

183-188

1 reference

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https://scigraph.springernature.com/pub.10.1038/eye.2001.57

7 November 2019

exact match

0 references

cites work

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

Cytochrome c oxidase mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

Cytochrome b mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutation

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2001.57

7 January 2021