doi.org/10.1093/hmg/8.8.1523, hdl.handle.net/1765/59949
Human Molecular Genetics
Department of Pediatrics

Houten, S. M., Romeijn, G., Koster, J., Gray, R. G. F., Darbyshire, P., Smit, G. P., … Waterham, H. R. (1999). Identification and characterization of three novel missense mutations in mevalonate kinase cDNA causing mevalonic aciduria, a disorder of isoprene biosynthesis. Human Molecular Genetics, 8(8), 1523–1528. doi:10.1093/hmg/8.8.1523