KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect
KCTD7 缺乏症是一种独特的神经退行性疾病，具有保守的自噬溶酶体缺陷
期刊:Annals of Neurology
影响因子:8.1
doi:10.1002/ana.25351
Kyle A Metz, Xinchen Teng, Isabelle Coppens, Heather M Lamb, Bart E Wagner, Jill A Rosenfeld, Xianghui Chen, Yu Zhang, Hee Jong Kim, Michael E Meadow, Tim Sen Wang, Edda D Haberlandt, Glenn W Anderson, Esther Leshinsky-Silver, Weimin Bi, Thomas C Markello, Marsha Pratt, Nawal Makhseed, Adolfo Garnic
信号转导
神经
细胞生物学
FCM
IF
IHC-P
Autophagy
GFP
