Hereditary spastic paraplegia with thin corpus callosum and SPG11 mutation: A neuropathological evaluation.
胼胝体变薄伴 SPG11 基因突变的遗传性痉挛性截瘫：神经病理学评估
期刊:Neuropathology
影响因子:1.2
doi:10.1111/neup.13007
Scherpelz Kathryn P, Yoda Rebecca A, Jayadev Suman, Davis Marie Y, Hincks Joshua C, Liachko Nicole F, Bragg Robert M, Cochoit Alexa, MacDonald Christine L, Keene C Dirk, Bird Thomas D, Latimer Caitlin S
