CAPN3 mutation c. 643-663del21 identified in 52 Norwegian...

Neuromuscular Disorders 2015 / 10 Vol. 25

CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy

Van Ghelue, M., Wahl, C., Arntzen, K., Loseth, S., Bindoff, L., Sveberg, L., Rosby, O., Popperud, T., Rasmussen, M., Halvorsen, H., Lindal, S., Jonsrud, C., Orstavik, K.
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Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.175
Date:
October, 2015
File:
PDF, 227 KB
english, 2015
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