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miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseases

Carrella, S; Di Guida, M; Brillante, S; Piccolo, D; Ciampi, L; Guadagnino, I; Piqueras, JG; Pizzo, M; Marrocco, E; Molinari, M; Petrogiannakis, G; Barbato, S; Ezhova, Y; Auricchio, A; Franco, B; De Leonibus, E; Surace, EM; Indrieri, A; Banfi, S

Carrella, S; Banfi, S (通讯作者),Telethon Inst Genet & Med TIGEM, Pozzuoli, Italy.;Carrella, S (通讯作者),Stn Zool Anton Dohrn, Ecosustainable Marine Biotechnol Dept, Naples, Italy.;Banfi, S (通讯作者),Univ Campania L Vanvitelli, Dept Precis Med, Med Genet, Naples, Italy.

EMBO MOLECULAR MEDICINE, 2022; 14 (11):

Abstract

Inherited retinal diseases (IRDs) are a group of diseases whose common landmark is progressive photoreceptor loss. The development of gene-specific th......

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