Dutch founder mutation in MICU1 found in seven patients with a LGMD-like phenotype and cognitive impairment

Author(s):
Ginjaar, I.; Niks, E.; Pol, L. van der; Kooi, A. van der; Straathof, C.; Duyvenvoorde, H. van; Kriek, M.
Published
2016
Publication type
Article / Letter to editor
Date issued
2016-10-31
Language
English
Is part of
Neuromuscular Disorders (2016), Vol. 26, p. S176-S176
hdl
1887/112635
doi
10.1016/j.nmd.2016.06.326