News at IFV

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Uppsala Mutation study is published

2021-08-13

Our Uppsala Mutation study is published in Science Translational Medicine:

M. Pagnon de la Vega, V. Giedraitis, W. Michno, L. Kilander, G. Güner, M. Zielinski, M. Löwenmark, R. Brundin, T. Danfors, L. Söderberg, I. Alafuzoff, L. N. Nilsson, A. Erlandsson, D. Willbold, S. A. Müller, G. F. Schröder, J. Hanrieder, S. F. Lichtenthaler, L. Lannfelt, D. Sehlin, M. Ingelsson, The Uppsala APP deletion causes early onset autosomal dominant Alzheimer’s disease by altering APP processing and increasing amyloid β fibril formation. Sci Transl Med. 2021 Aug 11;13 (606): eabc6184. doi: 10.1126/scitranslmed.abc6184. PMID: 34380771.

To access the article, please visit the Swedish version of this webpage.