(Q73785205)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

T Ferlin

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

P Landrieu

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

C Rambaud

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

H Fernandez

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

R Dumoulin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

P Rustin

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

B Mousson

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

language of work or name

English

0 references

publication date

1 September 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

6 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

131

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

447-449

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutation

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2980074-1

The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2980074-1

Biochemical and molecular investigations in respiratory chain deficiencies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2980074-1

Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2980074-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2980074-1

Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2980074-1

10.1016/S0022-3476(97)80074-1

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9329425%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference