ALG9/YNL219C Literature Guide Help

Other names published for ALG9: dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase, YNL219C

ALG9 - Disease Gene Related (3)

ReferenceOther Genes Addressed
Weinstein M, et al.  (2005) CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features. Am J Med Genet A 136(2):194-7
Frank CG, et al.  (2004) Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. Am J Hum Genet 75(1):146-50
Baysal BE, et al.  (2002) A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family. Neurogenetics 4(1):43-53