W. Frankhuizen

Local dystrophin restoration with antisense oligonucleotide PRO051.

Johan T den Dunnen, G. van Ommen, J. D. den Dunnen, 2007, The New England journal of medicine.

Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display

K. Bushby, R. Frants, S. Laval, 2005, European Journal of Human Genetics.

The insulin receptor tyrosine kinase domain in a chimaeric epidermal growth factor-insulin receptor generates Ca2+ signals through the PLC-gamma1 pathway.

P. Willems, W. Frankhuizen, J. Maassen, 1999, Biochimica et biophysica acta.

Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients

W. Linssen, C. Straathof, Ludo W van der Pol, 2019, Clinical genetics.

Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families

F. Spaans, P. Barth, A. Wintzen, 2007, Neurology.

Risk of erroneous results in carrier testing for haemophilia A without prior DNA analysis in male index patients

C. Ruivenkamp, D. E. Fransen van de Putte, E. Boon, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

P.182Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: the clinical and molecular spectrum of 244 patients

W. Linssen, C. Straathof, N. Voermans, 2019, Neuromuscular Disorders.

ANO5 mutations in the Dutch limb girdle muscular dystrophy population

C. Straathof, I. Ginjaar, P. Doorn, 2011, Neuromuscular Disorders.

ANO5 mutations in the Dutch limb girdle muscular dystrophy population

C. Straathof, I. Ginjaar, P. Doorn, 2011, Neuromuscular Disorders.