A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression

DSpace Repository

A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression

Author: Buerk, Katrin; Kaiser, Frank J.; Tennstedt, Stephanie; Schoels, Ludger; Kreuz, Friedmar R.; Wieland, Thomas; Stromf, Tim M.; Buettner, Thomas; Hollstein, Ronja; Braunholz, Diana; Plaschke, Jens; Gillessen-Kaesbach, Gabriele; Zuehlke, Christine
Tübinger Autor(en):
Schöls, Ludger
Strom, Tim M.
Published in: European Journal of Medical Genetics (2014), Bd. 57, H. 5, S. 207-211
Verlagsangabe: Elsevier Science Bv
Language: English
Full text: http://dx.doi.org/10.1016/j.ejmg.2014.01.005
ISSN: 1769-7212
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
Show full item record

This item appears in the following Collection(s)