Achromatopsia: Genetics and Gene Therapy

Achromatopsia (ACHM), also known as rod monochromatism or total color blindness, is an autosomal recessively inherited retinal disorder that affects the cones of the retina, the type of photoreceptors responsible for high-acuity daylight vision. ACHM is caused by pathogenic variants in one of six co...

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Detalles Bibliográficos
Autores principales: Michalakis, Stylianos, Gerhardt, Maximilian, Rudolph, Günther, Priglinger, Siegfried, Priglinger, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766373/
https://www.ncbi.nlm.nih.gov/pubmed/34860352
http://dx.doi.org/10.1007/s40291-021-00565-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766373/
https://www.ncbi.nlm.nih.gov/pubmed/34860352
http://dx.doi.org/10.1007/s40291-021-00565-z

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