It is worth pointing out that symptoms in TULP1 mutation RP are comparable with autoimmune retinopathies; however, some RP patients have early age of onset (~20 years old), rapid development, and reduced ERGs, while patients with presumed anti-TULP1 AIR or CAR are older and presented sudden loss of vision with rapid progression [28]. This evidence concerns the gene TULP1 and retinitis pigmentosa 1.