A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression
Titel:
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression
Auteur:
Bürk, Katrin Kaiser, Frank J. Tennstedt, Stephanie Schöls, Ludger Kreuz, Friedmar R. Wieland, Thomas Strom, Tim M. Büttner, Thomas Hollstein, Ronja Braunholz, Diana Plaschke, Jens Gillessen-Kaesbach, Gabriele Zühlke, Christine