APA (7th ed.) Citation

Fukao, T., Akiba, K., Goto, M., Kuwayama, N., Morita, M., Hori, T., . . . Hasegawa, Y. (2014). The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation. Journal of human genetics, 59(11), 609-614. https://doi.org/10.1038/jhg.2014.79

Chicago Style (17th ed.) Citation

Fukao, Toshiyuki, et al. "The First Case in Asia of 2-methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD10 Disease) with Atypical Presentation." Journal of Human Genetics 59, no. 11 (2014): 609-614. https://doi.org/10.1038/jhg.2014.79.

MLA (9th ed.) Citation

Fukao, Toshiyuki, et al. "The First Case in Asia of 2-methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD10 Disease) with Atypical Presentation." Journal of Human Genetics, vol. 59, no. 11, 2014, pp. 609-614, https://doi.org/10.1038/jhg.2014.79.