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Viral-mediated vision rescue of a novel AIPL1 cone-rod dystrophy model

Defects in aryl hydrocarbon receptor interacting protein-like1 (AIPL1) are associated with blinding diseases with a wide range of severity in humans. We examined the mechanism behind autosomal dominant cone-rod dystrophy (adCORD) caused by 12 base pair (bp) deletion at proline 351 of hAIPL1 (P351Δ12...

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Publicat a:Hum Mol Genet
Autors principals: Ku, Cristy A., Chiodo, Vince A., Boye, Sanford L., Hayes, Abigail, Goldberg, Andrew F.X., Hauswirth, William W., Ramamurthy, Visvanathan
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2015
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4357806/
https://ncbi.nlm.nih.gov/pubmed/25274777
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu487
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