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Form and Function of Photoreceptors in kcnv2 Mutant Zebrafish: Implications for the Human Disease KCNV2 Retinopathy
DownloadFall 2020
KCNV2 retinopathy is a rare inherited retinal disease caused by mutations in the gene KCNV2, which encodes the potassium channel subunit KV8.2. Expressed by photoreceptors, KV8.2 is a critical component for the efficient generation of a neural response to light. KCNV2 retinopathy is characterized...
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