Inherited retinal disorders (IRDs) result in severe visual impairments in children and adults. A challenge in the field of retinal degenerations is identifying mechanisms of photoreceptor cell death related to specific genetic mutations. Mutations in the gene TULP1 have been associated with two forms of IRDs. early-onset retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA). https://chefesquipmenters.shop/product-category/immersion-blenders/