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	1.	A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblasts. [electronic resource] by Schutgens, R B Wanders, R J Jakobs, C Arslan-Kirchner, M Miller, K Wieacker, P Hunnemann, D Hurter, P von Schutz, M Producer: 19950130 In: Journal of inherited metabolic disease vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism. [electronic resource] by Gootjes, Jeannette Schmohl, Frank Mooijer, Petra A W Dekker, Conny Mandel, Hanna Topcu, Meral Huemer, Martina Von Schütz, M Marquardt, Thorsten Smeitink, Jan A Waterham, Hans R Wanders, Ronald J A Producer: 20041025 In: Human mutation vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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