OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background

BACKGROUND: Leber's hereditary optic neuropathy (LHON) and autosomal dominant optic atrophy (ADOA) are the most frequent forms of hereditary optic neuropathies. LHON is associated with mitochondrial DNA (mtDNA) mutations whereas ADOA is mainly due to mutations in the OPA1 gene that encodes a mi...

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Détails bibliographiques
Auteurs principaux: Pierron, Denis, Ferré, Marc, Rocher, Christophe, Chevrollier, Arnaud, Murail, Pascal, Thoraval, Didier, Amati-Bonneau, Patrizia, Reynier, Pascal, Letellier, Thierry
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2009
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2726129/
https://ncbi.nlm.nih.gov/pubmed/19619285
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-70
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