A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy.

MLA

Sakiyama, Yusuke, et al. “A New Phenotype of Mitochondrial Disease Characterized by Familial Late-Onset Predominant Axial Myopathy and Encephalopathy.” Acta Neuropathologica, vol. 121, no. 6, June 2011, pp. 775–83. EBSCOhost, https://doi.org/10.1007/s00401-011-0818-y.

APA

Sakiyama, Y., Okamoto, Y., Higuchi, I., Inamori, Y., Sangatsuda, Y., Michizono, K., Watanabe, O., Hatakeyama, H., Goto, Y., Arimura, K., & Takashima, H. (2011). A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy. In Acta Neuropathologica (Vol. 121, Issue 6, pp. 775–783). https://doi.org/10.1007/s00401-011-0818-y

Chicago

Sakiyama, Yusuke, Yuji Okamoto, Itsuro Higuchi, Yukie Inamori, Yoko Sangatsuda, Kumiko Michizono, Osamu Watanabe, et al. 2011. “A New Phenotype of Mitochondrial Disease Characterized by Familial Late-Onset Predominant Axial Myopathy and Encephalopathy.” Acta Neuropathologica. Vol. 121. doi:10.1007/s00401-011-0818-y.