Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a Cathepsin D variant p.A58V

Autor: Ehling, Rainer1, Nosková, Lenka2, Stránecký, Viktor2, Hartmannová, Hana2, Přistoupilová, Anna2, Hodaňová, Kateřina2, Benke, Thomas1, Kovacs, Gabor G.3, Ströbel, Thomas3, Niedermüller, Ulrike4, Wagner, Michaela5, Nachbauer, Wolfgang1, Janecke, Andreas6, Budka, Herbert3, Boesch, Sylvia1 sylvia.boesch@i-med.ac.at, Kmoch, Stanislav2 skmoch@lf1.cuni.cz
Zdroj: Journal of the Neurological Sciences. Mar2013, Vol. 326 Issue 1/2, p75-82. 8p.
Databáze: Academic Search Ultimate
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