An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease.
Autosomal recessive retinal degenerative diseases cause visual impairment and blindness in both humans and dogs. Currently, no standard treatment is available, but pioneering gene therapy-based canine models have been instrumental for clinical trials in humans. To study a novel form of retinal degen...
Main Authors: | , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2019-03-01
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Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC6424408?pdf=render |