Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
Spatacsin 功能障碍导致 SPG11 连锁遗传性痉挛性截瘫的轴突病理
期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddu200
Francesc Pérez-Brangulí, Himanshu K Mishra, Iryna Prots, Steven Havlicek, Zacharias Kohl, Domenica Saul, Christine Rummel, Jonatan Dorca-Arevalo, Martin Regensburger, Daniela Graef, Elisabeth Sock, Juan Blasi, Teja W Groemer, Ursula Schlötzer-Schrehardt, Jürgen Winkler, Beate Winner