APTX:

Alberto Imarisio1, Andrea Pilotto2, Alessandro Lupini3

  • 1Department of Molecular Medicine, University of Pavia, Pavia, Italy; IRCCS Mondino Foundation, Pavia, Italy.

概括

罕见的APTX基因突变,通常会导致1型眼运动无力症的动脉缩,可能会影响多系统缩帕金森症 (MSA-P) 风险和73岁患者的呈现.