(Q24531271)

4 July 2017

0 references

A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians (English)

1 reference

Leber hereditary optic neuropathy

4 July 2017

main subject

1 reference

8

Marc St-Hilaire

0 references

Bernard Brais

11

object named as

Bernard Brais

0 references

Bertrand Desjardins

6

object named as

Bertrand Desjardins

1 reference

4 July 2017

1

Anne-Marie Laberge

1 reference

4 July 2017

Michele Jomphe

2

1 reference

4 July 2017

Louis Houde

3

1 reference

4 July 2017

Helene Vezina

4

1 reference

4 July 2017

Marc Tremblay

5

1 reference

4 July 2017

Damian Labuda

7

1 reference

4 July 2017

Carol Macmillan

9

1 reference

4 July 2017

Eric A Shoubridge

10

1 reference

4 July 2017

language of work or name

English

0 references

publication date

13 June 2005

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

77

1 reference

4 July 2017

issue

2

1 reference

4 July 2017

page(s)

313-317

1 reference

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

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Leber hereditary optic neuropathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Fragmentation of the Québec population genetic pool (Canada): evidence from the genetic contribution of founders per region in the 17th and 18th centuries

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Hereditary optic nerve atrophy. A clinical-genealogical status over Danish families with Leber disease

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224533

Leber's hereditary optic neuropathy--the spectrum of mitochondrial DNA mutations in Chinese patients

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15954041

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Diagnosis and prognosis of Leber's disease: incidence of spontaneous total recuperation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15954041

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/432491

1 reference

4 July 2017

1 reference

4 July 2017

1 reference