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ALG12 gene

Known as: dol-P-Man dependent alpha-1,6-mannosyltransferase, ECM39, dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichol alpha-1,6-mannosyltransferase 
National Institutes of Health

Papers overview

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2016
2016
Congenital disorders of glycosylation (CDGs) are disorders of abnormal protein glycosylation that affect multiple organ systems… Expand
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Review
2014
Review
2014
Congenital Disorder of Glycosylation type Ig (ALG12-CDG) is part of a group of autosomal recessive conditions caused by… Expand
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2005
2005
The regulated transport of proteins across the nuclear envelope occurs through nuclear pore complexes (NPCs), which are composed… Expand
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2004
2004
We have engineered Trypanosoma brucei with a novel mariner transposition system that allows large populations of mutant cells to… Expand
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