Progerin, an Aberrant Spliced Form of Lamin A, Is a Potential Therapeutic Target for HGPS

Kim, BH; Chung, YH; Woo, TG; Kang, SM; Park, S; Park, BJ

Park, BJ (通讯作者)，PRG S&T Co Ltd, Rare Dis R&D Ctr, Busan 46274, South Korea.;Park, BJ (通讯作者)，Pusan Natl Univ, Coll Nat Sci, Dept Mol Biol, Busan 46231, South Korea.

CELLS, 2023; 12 (18):

Abstract

Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disorder caused by the mutant protein progerin, which is expressed by the abn......

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