Muntau, A. C., Mayerhofer, P. U., Paton, B. C., Kammerer, S., & Roscher, A. A. (2000). Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G. The American Society of Human Genetics.

Muntau, Ania C., Peter U. Mayerhofer, Barbara C. Paton, Stefan Kammerer, and Adelbert A. Roscher. Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G. The American Society of Human Genetics, 2000.

Muntau, Ania C., et al. Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G. The American Society of Human Genetics, 2000.