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Published in 2022 at "Human molecular genetics"
DOI: 10.1093/hmg/ddac013
Abstract: Retinal diseases exhibit extensive genetic heterogeneity and complex etiology with varying onset and severity. Mutations in over 200 genes can lead to photoreceptor dysfunction and/or cell death in retinal neurodegeneration. To deduce molecular pathways that…
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Keywords:
cell death;
cell;
degeneration;
rd1 ... See more keywords