A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C

MLA

Ronald J.A. Wanders, et al. “A Novel PEX12 Mutation Identified as the Cause of a Peroxisomal Biogenesis Disorder with Mild Clinical Phenotype, Mild Biochemical Abnormalities in Fibroblasts and a Mosaic Catalase Immunofluorescence Pattern, Even at 40 Degrees C.” Journal of Human Genetics, vol. 52, no. 7, Dec. 2006. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....f5612649eff9456c41fe72dab80a4d9b&authtype=sso&custid=ns315887.

APA

Ronald J.A. Wanders, Stanley H. Korman, Avraham Zeharia, Merel S. Ebberink, Alisa Gutman, Hans R. Waterham, & Andreea Nissenkorn. (2006). A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C. Journal of Human Genetics, 52(7).

Chicago

Ronald J.A. Wanders, Stanley H. Korman, Avraham Zeharia, Merel S. Ebberink, Alisa Gutman, Hans R. Waterham, and Andreea Nissenkorn. 2006. “A Novel PEX12 Mutation Identified as the Cause of a Peroxisomal Biogenesis Disorder with Mild Clinical Phenotype, Mild Biochemical Abnormalities in Fibroblasts and a Mosaic Catalase Immunofluorescence Pattern, Even at 40 Degrees C.” Journal of Human Genetics 52 (7). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....f5612649eff9456c41fe72dab80a4d9b&authtype=sso&custid=ns315887.