bibliographicCitation |
Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T. Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency. Journal of Human Genetics. 2007 Oct 30;52(12):1040–3. doi: 10.1007/s10038-007-0211-9. |