Wim Wuyts
Department of Medical Genetics
University of Antwerp
Antwerp
Belgium
Name/email consistency: high
- Myopathy and phosphorylase kinase deficiency caused by a mutation in the PHKA1 gene. Wuyts, W., Reyniers, E., Ceuterick, C., Storm, K., de Barsy, T., Martin, J.J. Am. J. Med. Genet. A (2005)
- Somatic and gonadal mosaicism in Hutchinson-Gilford progeria. Wuyts, W., Biervliet, M., Reyniers, E., D'Apice, M.R., Novelli, G., Storm, K. Am. J. Med. Genet. A (2005)
- An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas. Wuyts, W., Radersma, R., Storm, K., Vits, L. Clin. Genet. (2005)









