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Progeria study finds base-editing therapy lengthens lifespan in mice
Jan 27, 2021
harvard.edu
Medicina | Medical | Doctor | Dr on Instagram: "Estas niñas padecen del Síndrome de Progeria de Hutchinson-Gilford, también conocido como progeria infantil es una enfermedad genética rara, caracterizada por un envejecimiento prematuro que comienza tempranamente en la infancia. Las características fenotípicas de este síndrome son causadas por alteraciones en la proteína de la lámina A, componente fibrilar principal que mantiene la estructura del núcleo y participa en la organización de la cromati
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