(Q70698752)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

mitochondrial myopathy

1 reference

Y Shoji

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

W Sato

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

K Hayasaka

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

G Takada

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

publication date

1 January 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

13 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

27-30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00711311

13 October 2019

exact match

0 references

cites work

Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

1 reference

12 December 2020

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

1 reference

12 December 2020

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

1 reference

12 December 2020

A specific point mutation in the mitochondrial genome of Caucasians with MELAS

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

12 December 2020

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene

1 reference

12 December 2020

MELAS: clinical features, biochemistry, and molecular genetics

1 reference

12 December 2020

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

1 reference

12 December 2020

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00711311

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8487499%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference