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 |
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Zdroj: | Journal of the Neurological Sciences. Mar2013, Vol. 326 Issue 1/2, p75-82. 8p. |
Databáze: | Academic Search Ultimate |
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