Laddar...

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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Hum Mol Genet
Huvudupphovsmän: Ku, Cristy A., Chiodo, Vince A., Boye, Sanford L., Hayes, Abigail, Goldberg, Andrew F.X., Hauswirth, William W., Ramamurthy, Visvanathan
Materialtyp: Artigo
Språk:Inglês
Publicerad: Oxford University Press 2015
Ämnen:
Länkar: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
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!