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Published in 2017 at "Human Molecular Genetics"
DOI: 10.1093/hmg/ddx137
Abstract: In humans, CERKL mutations cause widespread retinal degeneration: early dysfunction and loss of rod and cone photoreceptors in the outer retina and, progressively, death of cells in the inner retina. Despite intensive efforts, the function…
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Keywords:
phagocytosis;
dystrophy;
photoreceptor outer;
rod cone ... See more keywords