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Dutch founder mutation in MICU1 found in seven patients with a LGMD-like phenotype and cognitive impairment
Ginjaar, I., Niks, E., van der Pol, L., van der Kooi, A., Straathof, C., van Duyvenvoorde, H., Kriek, M.Volume:
26
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2016.06.326
Date:
October, 2016
File:
PDF, 195 KB
english, 2016