Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency

1999-09-01

Human Genetics , Volume 105 - Issue 1-2 p. 157- 161

Additional Metadata
Persistent URL	doi.org/10.1007/s004390051079, hdl.handle.net/1765/56462
Journal	Human Genetics
Organisation	Department of Biochemistry
Citation APA Style AAA Style APA 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	Vaz, F., Scholte, H., Ruiter, J., Hussaarts-Odijk, L., Rodrigues Pereira, R., Schweitzer, S., … Wanders, R. (1999). Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency. Human Genetics, 105(1-2), 157–161. doi:10.1007/s004390051079

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