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	1.	Identification and characterization of the mouse cDNA encoding acyl-CoA:dihydroxyacetone phosphate acyltransferase. [electronic resource] by Ofman, R Hogenhout, E M Wanders, R J Producer: 19990811 In: Biochimica et biophysica acta vol. 1439 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Phytanoyl-CoA hydroxylase deficiency. Enzymological and molecular basis of classical Refsum disease. [electronic resource] by Jansen, G A Ferdinandusse, S Hogenhout, E M Verhoeven, N M Jakobs, C Wanders, R J Producer: 20000411 In: Advances in experimental medicine and biology vol. 466 Availability: No items available. Save to lists Add to cart (remove)
	3.	Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2. [electronic resource] by Ofman, R Hettema, E H Hogenhout, E M Caruso, U Muijsers, A O Wanders, R J Producer: 19980826 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Phytanoyl-CoA hydroxylase from rat liver. Protein purification and cDNA cloning with implications for the subcellular localization of phytanic acid alpha-oxidation. [electronic resource] by Jansen, G A Ofman, R Denis, S Ferdinandusse, S Hogenhout, E M Jakobs, C Wanders, R J Producer: 20000210 In: Journal of lipid research vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	5.	Human phytanoyl-CoA hydroxylase: resolution of the gene structure and the molecular basis of Refsum's disease. [electronic resource] by Jansen, G A Hogenhout, E M Ferdinandusse, S Waterham, H R Ofman, R Jakobs, C Skjeldal, O H Wanders, R J Producer: 20000623 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Molecular basis of rhizomelic chondrodysplasia punctata type I: high frequency of the Leu-292 stop mutation in 38 patients. [electronic resource] by Brites, P Motley, A Hogenhout, E Hettema, E Wijburg, F Heijmans, H S Tabak, H F Distel, B Wanders, R J Producer: 19981104 In: Journal of inherited metabolic disease vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein. [electronic resource] by Ferdinandusse, S van Grunsven, E G Oostheim, W Denis, S Hogenhout, E M IJlst, L van Roermund, C W T Waterham, H R Goldfischer, S Wanders, R J A Producer: 20020627 In: American journal of human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor. [electronic resource] by Motley, A M Hettema, E H Hogenhout, E M Brites, P ten Asbroek, A L Wijburg, F A Baas, F Heijmans, H S Tabak, H F Wanders, R J Distel, B Producer: 19970425 In: Nature genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)