(Q70669999)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

K D Gerbitz

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

A Paprotta

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

M Jaksch

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

S Zierz

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

J Drechsel

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

language of work or name

English

0 references

publication date

1 April 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

321

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

2-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

194-196

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

13 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

Does the mitochondrial DNA play a role in the pathogenesis of diabetes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2893%2980106-5

10.1016/0014-5793(93)80106-5

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8477849%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference