Persistent URL of this record https://hdl.handle.net/1887/112635
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Dutch founder mutation in MICU1 found in seven patients with a LGMD-like phenotype and cognitive impairment
- All authors
- Ginjaar, I.; Niks, E.; Pol, L. van der; Kooi, A. van der; Straathof, C.; Duyvenvoorde, H. van; Kriek, M.
- Date
- 2016-10-31
- Journal
- Neuromuscular Disorders
- Volume
- 26
- Pages
- S176 - S176