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Gene Therapy for Color Blindness

Achromatopsia is a rare congenital cause of vision loss due to isolated cone photoreceptor dysfunction. The most common underlying genetic mutations are autosomal recessive changes in CNGA3, CNGB3, GNAT2, PDE6H, PDE6C, or ATF6. Animal models of Cnga3, Cngb3, and Gnat2 have been rescued using AAV gen...

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Bibliografski detalji
Izdano u:Yale J Biol Med
Glavni autori: Hassall, Mark M., Barnard, Alun R., MacLaren, Robert E.
Format: Artigo
Jezik:Inglês
Izdano: YJBM 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5733843/
https://ncbi.nlm.nih.gov/pubmed/29259520
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