(Q72231129)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

hereditary optic neuropathy

25 October 2019

main subject

1 reference

Y Mashima

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

Y Hiida

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

Y Oguchi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

J Kudoh

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

N Shimizu

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

publication date

1 August 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

volume

92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

page(s)

101-102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00216156

25 October 2019

exact match

0 references

cites work

Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism

1 reference

12 December 2020

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy

1 reference

12 December 2020

Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy

1 reference

12 December 2020

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

1 reference

12 December 2020

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.

1 reference

12 December 2020

Mitochondrial DNA analysis of Leber's hereditary optic neuropathy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00216156

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103501%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference