APA

Yamashita T., Mitsui J., Shimozawa N., Takashima S., Umemura H., Sato K., Takemoto M., Hishikawa N., Ohta Y., Matsukawa T., Ishiura H., Yoshimura J., Doi K., Morishita S., Tsuji S. & Abe K. (20170705). Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype. : Journal of the neurological sciences.

Chicago

Yamashita Toru, Mitsui Jun, Shimozawa Nobuyuki, Takashima Shigeo, Umemura Hiroshi, Sato Kota, Takemoto Mami, Hishikawa Nozomi, Ohta Yasuyuki, Matsukawa Takashi, Ishiura Hiroyuki, Yoshimura Jun, Doi Koichiro, Morishita Shinichi, Tsuji Shoji and Abe Koji. 20170705. Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype. : Journal of the neurological sciences.

Harvard

Yamashita T., Mitsui J., Shimozawa N., Takashima S., Umemura H., Sato K., Takemoto M., Hishikawa N., Ohta Y., Matsukawa T., Ishiura H., Yoshimura J., Doi K., Morishita S., Tsuji S. and Abe K. (20170705). Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype. : Journal of the neurological sciences.

MLA

Yamashita Toru, Mitsui Jun, Shimozawa Nobuyuki, Takashima Shigeo, Umemura Hiroshi, Sato Kota, Takemoto Mami, Hishikawa Nozomi, Ohta Yasuyuki, Matsukawa Takashi, Ishiura Hiroyuki, Yoshimura Jun, Doi Koichiro, Morishita Shinichi, Tsuji Shoji and Abe Koji. Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype. : Journal of the neurological sciences. 20170705.