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	1.	ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg. [electronic resource] by Grubenmann, Claudia E Frank, Christian G Kjaergaard, Susanne Berger, Eric G Aebi, Markus Hennet, Thierry Producer: 20030414 In: Human molecular genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. [electronic resource] by Frank, Christian G Grubenmann, Claudia E Eyaid, Wafaa Berger, Eric G Aebi, Markus Hennet, Thierry Producer: 20040720 In: American journal of human genetics vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik. [electronic resource] by Grubenmann, Claudia E Frank, Christian G Hülsmeier, Andreas J Schollen, Els Matthijs, Gert Mayatepek, Ertan Berger, Eric G Aebi, Markus Hennet, Thierry Producer: 20041207 In: Human molecular genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features. [electronic resource] by Weinstein, Michael Schollen, Els Matthijs, Gert Neupert, Christine Hennet, Thierry Grubenmann, Claudia E Frank, Christian G Aebi, Markus Clarke, Joe T R Griffiths, Anne Seargeant, Lorne Poplawski, Nicola Producer: 20050914 In: American journal of medical genetics. Part A vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)