Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia
CPT1C功能缺失变异:不支持其在遗传性痉挛性截瘫中起因果作用
期刊:Movement Disorders
影响因子:7.6
doi:10.1002/mds.70144
Zhu, Rui; Liu, Lang; Estiar, Mehrdad A; Asayesh, Farnaz; Ahmad, Jamil; Teferra, Meron; Yoon, Grace; Tarnopolsky, Mark; Boycott, Kym M; Dupre, Nicolas; Dion, Patrick A; Suchowersky, Oksana; Jordanova, Albena; Lee, Yi-Chung; Stevanin, Giovanni; Zuchner, Stephan; Rouleau, Guy A; Gan-Or, Ziv