Mutation in Wdr45 leads to early motor dysfunction and widespread aberrant axon terminals in a beta-propeller protein associated neurodegeneration (BPAN) patient-inspired mouse model
Wdr45 基因突变会导致 β-螺旋桨蛋白相关神经退行性疾病 (BPAN) 患者模型中出现早期运动功能障碍和广泛的异常轴突末梢。
期刊:Frontiers in Neuroscience
影响因子:3.2
doi:10.3389/fnins.2025.1545004
Meyerink, Brandon L; Karia, Krishna S; Rechtzigel, Mitchell J; Patthi, Prithvi R; Edwards, Ariana C; Howard, Jessica M; Aaseng, Elizabeth R; Aftab, Shamiq; Weimer, Jill M; Pilaz, Louis-Jan
