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.
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A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family
Mengel, D.; Liu, L.; Yamamoto, R.; Zülow, S.; Deuschl, C.; Hermann, D. M. & Zerr, I. et al. (2020)
Neurobiology of Aging, 85 pp. 154.e5-154.e7. DOI: https://doi.org/10.1016/j.neurobiolaging.2019.07.002
