(Q81797014)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

title

[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

author name string

C Verny

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

P Amati-Bonneau

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

F Dubas

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Y Malthiéry

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

D Bonneau

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

publication date

1 April 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

volume

161

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

page(s)

451-454

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

12 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2805%2985075-1

7 January 2021

Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2805%2985075-1

7 January 2021

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2805%2985075-1

7 January 2021

Ueber degenerative Atrophie der spinalen Hinterstränge

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2805%2985075-1

7 January 2021

OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2805%2985075-1

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2805%2985075-1

7 January 2021

10.1016/S0035-3787(05)85075-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15924081%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference