A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family
2020 | journal article. A publication with affiliation to the University of Göttingen.
Jump to: Cite & Linked | Documents & Media | Details | Version history
Cite this publication
Mengel, David, et al. "A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family." Neurobiology of Aging, vol. 85, 2020, pp. 154.e5-154.e7, doi: 10.1016/j.neurobiolaging.2019.07.002.
