(Q46581648)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18496845%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Hereditary optic neuropathies share a common mitochondrial coupling defect (English)

1 reference

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7 January 2020

7

1 reference

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7 January 2020

Vincent Procaccio

13

1 reference

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7 January 2020

Pascal Reynier

15

1 reference

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7 January 2020

Patrizia Amati-Bonneau

12

object named as

Patrizia Amati-Bonneau

1 reference

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7 January 2020

6

Christophe Verny

1 reference

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7 January 2020

author name string

Arnaud Chevrollier

1

1 reference

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7 January 2020

Virginie Guillet

2

1 reference

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7 January 2020

Dominique Loiseau

3

1 reference

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7 January 2020

Naïg Gueguen

4

1 reference

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7 January 2020

Marie-Anne Pou de Crescenzo

5

1 reference

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7 January 2020

Hélène Dollfus

8

1 reference

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7 January 2020

Sylvie Odent

9

1 reference

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7 January 2020

Dan Milea

10

1 reference

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7 January 2020

Cyril Goizet

11

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7 January 2020

Dominique Bonneau

14

1 reference

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7 January 2020

publication date

1 June 2008

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7 January 2020

1 reference

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7 January 2020

volume

63

1 reference

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7 January 2020

issue

6

1 reference

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7 January 2020

page(s)

794-798

1 reference

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Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome.

7 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.21385

21 January 2018

Identifiers

DOI

10.1002/ANA.21385

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18496845%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference