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	1.	Late onset Krabbe disease due to the new GALC p.Ala543Pro mutation, with intriguingly high residual GALC activity in vitro. [electronic resource] by Krägeloh-Mann, Inge Harzer, Klaus Rostásy, Kevin Beck-Wödl, Stefanie Bornemann, Antje Böhringer, Judith Bevot, Andrea Beck, Verena Merkel, Gisela Pechan, Maria Producer: 20171221 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Enzymatic characterization of novel arylsulfatase A variants using human arylsulfatase A-deficient immortalized mesenchymal stromal cells. [electronic resource] by Böhringer, Judith Santer, René Schumacher, Neele Gieseke, Friederike Cornils, Kerstin Pechan, Maria Kustermann-Kuhn, Birgit Handgretinger, Rupert Schöls, Ludger Harzer, Klaus Krägeloh-Mann, Ingeborg Müller, Ingo Producer: 20180530 In: Human mutation vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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