(Q74014562)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

2

1 reference

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8 November 2019

Miguel Angel Martín

6

1 reference

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8 November 2019

Joaquín Arenas

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

Y Campos

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

A García

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

A L Andreu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

J C Rubio

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

P del Hoyo

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

C Navarro

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

C Cervera

9

1 reference

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8 November 2019

R Garesse

10

1 reference

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8 November 2019

publication date

1 July 2001

1 reference

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8 November 2019

published in

Neuromuscular Disorders

1 reference

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8 November 2019

volume

11

1 reference

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8 November 2019

issue

5

1 reference

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8 November 2019

page(s)

477-480

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

Mitochondrial DNA mutations and pathogenesis

8 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900223-6

7 January 2021

Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900223-6

7 January 2021

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900223-6

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900223-6

7 January 2021

Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900223-6

7 January 2021

A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn).

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900223-6

7 January 2021

10.1016/S0960-8966(00)00223-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11404120%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference