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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Detalhes bibliográficos
Principais autores: Pierron, Denis, Ferré, Marc, Rocher, Christophe, Chevrollier, Arnaud, Murail, Pascal, Thoraval, Didier, Amati-Bonneau, Patrizia, Reynier, Pascal, Letellier, Thierry
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
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Research Article
Acesso em linha: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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