![](/img/cover-not-exists.png)
Molecular basis of stiff patient syndrome caused by mutations in ACTA1 and TPM3
Papadaki, M., Marston, S., Memo, M., Messer, A., Donkervoort, S., Bönnemann, C., Nowak, K., Ong, R., McNamara, E.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.359
Date:
October, 2015
File:
PDF, 209 KB
english, 2015