Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology
RAB39B 突变可导致 X 连锁智力障碍和伴有 α-突触核蛋白病理的早发性帕金森病
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2014.10.015
Gabrielle R Wilson, Joe C H Sim, Catriona McLean, Maila Giannandrea, Charles A Galea, Jessica R Riseley, Sarah E M Stephenson, Elizabeth Fitzpatrick, Stefan A Haas, Kate Pope, Kirk J Hogan, Ronald G Gregg, Catherine J Bromhead, David S Wargowski, Christopher H Lawrence, Paul A James, Andrew Churchya
