Alpha-1,2-mannosyltransferase ALG9
Definition:
References:
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[1]. Michael Weinstein, et al. CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features. Am J Med Genet A. 2005 Jul 15;136(2):194-7. [Content Brief]
[2]. Christian G Frank, et al. Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. Am J Hum Genet. 2004 Jul;75(1):146-50. [Content Brief]