Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy

OBJECTIVE: To improve the genetic diagnosis of dominant optic atrophy (DOA), the most frequently inherited optic nerve disease, and infer genotype-phenotype correlations. METHODS: Exonic sequences of 22 genes were screened by new-generation sequencing in patients with DOA who were investigated for o...

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Publicado en:Neurol Genet
Autores principales: Charif, Majida, Chevrollier, Arnaud, Gueguen, Naïg, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valérie, Leruez, Stéphanie, Colin, Estelle, Meunier, Audrey, Vignal, Catherine, Smirnov, Vasily, Defoort-Dhellemmes, Sabine, Drumare Bouvet, Isabelle, Goizet, Cyril, Votruba, Marcela, Jurkute, Neringa, Yu-Wai-Man, Patrick, Tagliavini, Francesca, Caporali, Leonardo, La Morgia, Chiara, Carelli, Valerio, Procaccio, Vincent, Zanlonghi, Xavier, Meunier, Isabelle, Reynier, Pascal, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy
Formato: Artigo
Lenguaje:Inglês
Publicado: Wolters Kluwer 2020
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7251510/
https://ncbi.nlm.nih.gov/pubmed/32548275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000428
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