(Q79314462)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

title

Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

1 reference

Leber hereditary optic neuropathy

1 reference

inferred from title

author name string

Nopasak Phasukkijwatana

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Wanicha L Chuenkongkaew

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Rungnapa Suphavilai

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Komon Luangtrakool

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Bussaraporn Kunhapan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Patcharee Lertrit

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

publication date

28 October 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

21 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

page(s)

1110-1117

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17072496%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10038-006-0073-6

21 December 2019

exact match

0 references

cites work

Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient

1 reference

12 December 2020

Leber's hereditary optic neuropathy in Thailand

1 reference

12 December 2020

Leber hereditary optic neuropathy: clinical and molecular genetic findings

1 reference

12 December 2020

Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing

1 reference

12 December 2020

Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

1 reference

12 December 2020

The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees

1 reference

12 December 2020

mtDNA mutations in Leber's hereditary optic neuropathy

1 reference

12 December 2020

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

1 reference

12 December 2020

Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.

1 reference

12 December 2020

Leber hereditary optic neuropathy

1 reference

12 December 2020

The epidemiology of Leber hereditary optic neuropathy in the North East of England

1 reference

12 December 2020

An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy

1 reference

12 December 2020

Nuclear genetic control of mitochondrial DNA segregation

1 reference

12 December 2020

Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigree

1 reference

12 December 2020

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

12 December 2020

Low-penetrance branches in matrilineal pedigrees with Leber 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

Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy

1 reference

12 December 2020

Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation

1 reference

12 December 2020

Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy

1 reference

12 December 2020

A heteroplasmic LHON family: tissue distribution and transmission of the 11778 mutation.

1 reference

12 December 2020

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

1 reference

12 December 2020

Heteroplasmy in Leber's hereditary optic neuropathy

1 reference

12 December 2020

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

1 reference

12 December 2020