A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13

MLA

Barøy, T., et al. “A Novel Mutation in FBXL4 in a Norwegian Child with Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13.” European Journal of Medical Genetics, 2016. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1367167230&authtype=sso&custid=ns315887.

APA

Barøy, T., Pedurupillay, C. R., Bliksrud, Y. T., Rasmussen, M., Holmgren, A., Vigeland, M. D., Hughes, T., Brink, M., Rodenburg, R. J. T., Nedregaard, B., Strømme, P., Frengen, E., & Misceo, D. (2016). A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13. European Journal of Medical Genetics.

Chicago

Barøy, T., C.R. Pedurupillay, Y.T. Bliksrud, M. Rasmussen, A. Holmgren, M.D. Vigeland, T. Hughes, et al. 2016. “A Novel Mutation in FBXL4 in a Norwegian Child with Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13.” European Journal of Medical Genetics. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1367167230&authtype=sso&custid=ns315887.