Restoration of Cone Vision in the CNGA3(−/−) Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function

Congenital absence of cone photoreceptor function is associated with strongly impaired daylight vision and loss of color discrimination in human achromatopsia. Here, we introduce viral gene replacement therapy as a potential treatment for this disease in the CNGA3(−/−) mouse model. We show that such...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Michalakis, Stylianos, Mühlfriedel, Regine, Tanimoto, Naoyuki, Krishnamoorthy, Vidhyasankar, Koch, Susanne, Fischer, M Dominik, Becirovic, Elvir, Bai, Lin, Huber, Gesine, Beck, Susanne C, Fahl, Edda, Büning, Hildegard, Paquet-Durand, François, Zong, Xiangang, Gollisch, Tim, Biel, Martin, Seeliger, Mathias W
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2010
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2997579/
https://ncbi.nlm.nih.gov/pubmed/20628362
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mt.2010.149
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados