(Q61922622)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

Neuromuscular syndrome associated with the 3291T-->C mutation of mitochondrial DNA: a second case (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

Eleonora Lamantea

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

Marina Mora

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

G Uziel

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

F Carrara

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

M Zeviani

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

publication date

1 August 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

published in

Neuromuscular Disorders

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

page(s)

415-418

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

Molecular genetic aspects of human mitochondrial disorders

8 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7

7 January 2021

A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7

7 January 2021

A novel mutation (8342G→A) in the mitochondrial tRNALys gene associated with progressive external ophthalmoplegia and myoclonus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7

7 January 2021

A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7

7 January 2021

10.1016/S0960-8966(99)00115-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference