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

Katrin Bürk, Frank J. Kaiser, Stephanie Tennstedt, Ludger Schöls, Friedmar R. Kreuz, Thomas Wieland, Tim M. Strom, Thomas Büttner, Ronja Hollstein, Diana Braunholz, Jens Plaschke, Gabriele Gillessen-Kaesbach, Christine Zühlke*

*Corresponding author for this work
7 Citations (Scopus)

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Neuroscience

Biochemistry, Genetics and Molecular Biology