New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G...
New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation
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Author / Creator
Pierron, Denis , Rocher, Christophe , Amati-Bonneau, Patricia , Reynier, Pascal , Martin-Négrier, Marie-Laure , Allouche, Stéphane , Batandier, Cécile , Mousson de Camaret, Benedicte , Godinot, Catherine , Rotig, Agnes , Feldmann, Delphine , Bellanne-Chantelot, Christine , Arveiler, Benoit , Pennarun, Erwann , Rossignol, Rodrigue , Crouzet, Marc , Murail, Pascal , Thoraval, Didier and Letellier, Thierry
Publisher
England: BioMed Central Ltd
Journal title
Language
English
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Publication information
Publisher
England: BioMed Central Ltd
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Scope and Contents
Contents
The A3243G mutation in the tRNALeu gene (UUR), is one of the most common pathogenic mitochondrial DNA (mtDNA) mutations in France, and is associated with highly variable and heterogeneous disease phenotypes. To define the relationships between the A3243G mutation and mtDNA backgrounds, we determined the haplogroup affiliation of 142 unrelated Frenc...
Alternative Titles
Full title
New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation
Authors, Artists and Contributors
Author / Creator
Rocher, Christophe
Amati-Bonneau, Patricia
Reynier, Pascal
Martin-Négrier, Marie-Laure
Allouche, Stéphane
Batandier, Cécile
Mousson de Camaret, Benedicte
Godinot, Catherine
Rotig, Agnes
Feldmann, Delphine
Bellanne-Chantelot, Christine
Arveiler, Benoit
Pennarun, Erwann
Rossignol, Rodrigue
Crouzet, Marc
Murail, Pascal
Thoraval, Didier
Letellier, Thierry
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Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_1e0a95568fbf407c97d688a3914f0b5f
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1e0a95568fbf407c97d688a3914f0b5f
Other Identifiers
ISSN
1471-2350
E-ISSN
1471-2350
DOI
10.1186/1471-2350-9-41
