Tamura, S., Okumoto, K., Toyama, R., Shimozawa, N., Tsukamoto, T., Suzuki, Y., . . . Fujiki, Y. (1998). Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I. The National Academy of Sciences.

Tamura, Shigehiko, Kanji Okumoto, Ryusuke Toyama, Nobuyuki Shimozawa, Toshiro Tsukamoto, Yasuyuki Suzuki, Takashi Osumi, Naomi Kondo, and Yukio Fujiki. Human PEX1 Cloned By Functional Complementation On a CHO Cell Mutant Is Responsible for Peroxisome-deficient Zellweger Syndrome of Complementation Group I. The National Academy of Sciences, 1998.

Tamura, Shigehiko, et al. Human PEX1 Cloned By Functional Complementation On a CHO Cell Mutant Is Responsible for Peroxisome-deficient Zellweger Syndrome of Complementation Group I. The National Academy of Sciences, 1998.