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Pol, L. van der
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Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients
Dutch founder mutation in MICU1 found in seven patients with a LGMD-like phenotype and cognitive impairment
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling
Brain natriuretic peptide is not predictive of dilated cardiomyopathy in Becker and Duchenne muscular dystrophy patients and carriers
Novel missense mutations in the glycine receptor beta subunit gene (GLRB) in startle disease
Inter- and intra muscle fat fraction variability in DMD patients