Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

作者：Alfredo Ramı́rez, André Heimbach, Jan Gründemann, Barbara Stiller, D. J Hampshire, L. Pablo Cid, Ingrid Goebel, Ammar Fayez Mubaidin, Abdul-Latif Wriekat, Jochen Roeper, Amir S. Najim Al-Din, Axel M. Hillmer, Meliha Karsak, Birgit Liss, Christopher Geoffrey Woods, María Isabel Behrens, Christian Kubisch · 发表于：Nature Genetics · 年份：2006 · DOI：10.1038/ng1884 · 被引用次数：1212 · 研究领域：Cellular transport and secretion、Lysosomal Storage Disorders Research、Endoplasmic Reticulum Stress and Disease