Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a Cathepsin D variant p.A58V-Reference-Cited by-同舟云学术

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

Published:2013-03 Issue:1-2 Volume:326 Page:75-82
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Ehling Rainer,Nosková Lenka,Stránecký Viktor,Hartmannová Hana,Přistoupilová Anna,Hodaňová Kateřina,Benke Thomas,Kovacs Gabor G.,Ströbel Thomas,Niedermüller Ulrike,Wagner Michaela,Nachbauer Wolfgang,Janecke Andreas,Budka Herbert,Boesch Sylvia,Kmoch Stanislav

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference32 articles.

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