APA

Steinberg S. J., Snowden A., Braverman N. E., Chen L., Watkins P. A., Clayton P. T., Setchell K. D. R., Heubi J. E., Raymond G. V., Moser A. B. & Moser H. W. (20090522). A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts. : Journal of inherited metabolic disease.

Chicago

Steinberg S J, Snowden A, Braverman N E, Chen L, Watkins P A, Clayton P T, Setchell K D R, Heubi J E, Raymond G V, Moser A B and Moser H W. 20090522. A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts. : Journal of inherited metabolic disease.

Harvard

Steinberg S. J., Snowden A., Braverman N. E., Chen L., Watkins P. A., Clayton P. T., Setchell K. D. R., Heubi J. E., Raymond G. V., Moser A. B. and Moser H. W. (20090522). A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts. : Journal of inherited metabolic disease.

MLA

Steinberg S J, Snowden A, Braverman N E, Chen L, Watkins P A, Clayton P T, Setchell K D R, Heubi J E, Raymond G V, Moser A B and Moser H W. A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts. : Journal of inherited metabolic disease. 20090522.