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Genetic Factors of Eye Disease: Retinitis Pigmentosa (RP) & the RHO Gene
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Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous blinding retinal disease, which belongs to the large group of inherited retinal diseases —for which 54 retinal genes have been found to be mutated thus far. RP commences with progressive night blindness due to rod photoreceptor disease, accompanied by gradual loss of peripheral visual field, followed by complete blindness due to cone photoreceptor degeneration.
RHO (Rhodopsin) is a Protein Coding gene. The rhodopsin protein encoded by the RHO gene is found in rod cells in the back of the eye and is essential for vision in low-light conditions.
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RHO (Rhodopsin) is a Protein Coding gene. The rhodopsin protein encoded by the RHO gene is found in rod cells in the back of the eye and is essential for vision in low-light conditions.
【PS. : Comment with your answer. Truth would be revealed in next video】
【Don’t wanna miss any of this content? 】
【Be sure to SUBSCRIBE to Cyagen for new videos like this one every two weeks!!】
Follow us on Social Media:
Email：
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