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