C8ORF37
C8ORF37 (Chromosome 8 Open Reading Frame 37): C8ORF37 is a gene associated with retinal dystrophies and Bardet-Biedl syndrome — a condition characterised by vision loss, obesity, and other symptoms. It plays a crucial role in maintaining photoreceptor cells and supporting cilia-related processes. Mutations in this gene can lead to retinal degeneration and disrupt normal ciliary function.
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