APA citiranje

Honsho, M., Tamura, S., Shimozawa, N., Suzuki, Y., Kondo, N., & Fujiki, Y. (1998). Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Citação norma Chicago

Honsho, M., S. Tamura, N. Shimozawa, Y. Suzuki, N. Kondo, and Y. Fujiki. Mutation in PEX16 Is Causal in the Peroxisome-deficient Zellweger Syndrome of Complementation Group D. 1998.

MLA citiranje

Honsho, M., et al. Mutation in PEX16 Is Causal in the Peroxisome-deficient Zellweger Syndrome of Complementation Group D. 1998.