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Blinded by the light: a nonhuman primate model of achromatopsia

Achromatopsia is an inherited retinal degeneration characterized by the loss of cone photoreceptor function. In this issue of the JCI, Moshiri et al. characterize a naturally occurring model of the disease in the rhesus macaque caused by homozygous mutations in the phototransduction enzyme PDE6C. Us...

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Detalhes bibliográficos
Publicado no:J Clin Invest
Main Authors: Uyhazi, Katherine E., Bennett, Jean
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6355213/
https://ncbi.nlm.nih.gov/pubmed/30667378
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI126205
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