Identification and characterization of three novel missense mutations in mevalonate kinase cDNA causing mevalonic aciduria, a disorder of isoprene biosynthesis

1999-08-18

Human Molecular Genetics , Volume 8 - Issue 8 p. 1523- 1528

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Persistent URL	doi.org/10.1093/hmg/8.8.1523, hdl.handle.net/1765/59949
Journal	Human Molecular Genetics
Organisation	Department of Pediatrics
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Houten, S. M., Romeijn, G., Koster, J., Gray, R. G. F., Darbyshire, P., Smit, G. P., de Klerk, J., Duran, M., Gibson, K. M., Wanders, R.& 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.https://doi.org/10.1093/hmg/8.8.1523

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