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Progeria: A Genetic and Rare Disease

Anitha Nandagopal*, Naaz Nazmeen, Firdous Afshan, Anupama Koneru Department of Pharmacology, Sultan-ul-Uloom College of Pharmacy, Road no.3, Banjara Hills, Hyderabad, Telangana-500034. ABSTRACT Hutchinson Gilford Progeria Syndrome is an extremely serious disorder characterized by rapid, premature ageing of children which can precipitate cardiovascular diseases. Progeria is caused by de novo mutation in Lamin A gene which activates splicing in donor site, ... Read More »

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