Matches in Nanopublications for { ?s ?p "[The congenital disorder of glycosylation (CDG)-Ic (ALG6-CDG, CDG-Ic) is caused by mutations in the hALG6 gene that encodes the N-glycosylation pathway enzyme, α-1,3-glucosyltransferase (NP_037471.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion description "[The congenital disorder of glycosylation (CDG)-Ic (ALG6-CDG, CDG-Ic) is caused by mutations in the hALG6 gene that encodes the N-glycosylation pathway enzyme, α-1,3-glucosyltransferase (NP_037471.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_provenance.
- NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_assertion description "[The congenital disorder of glycosylation (CDG)-Ic (ALG6-CDG, CDG-Ic) is caused by mutations in the hALG6 gene that encodes the N-glycosylation pathway enzyme, α-1,3-glucosyltransferase (NP_037471.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- NP253795.RA-O1_g_9nxIY1xAgXUpdujnJIk0RHwLhxFWh66mC9gvg130_assertion description "[The congenital disorder of glycosylation (CDG)-Ic (ALG6-CDG, CDG-Ic) is caused by mutations in the hALG6 gene that encodes the N-glycosylation pathway enzyme, α-1,3-glucosyltransferase (NP_037471.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253795.RA-O1_g_9nxIY1xAgXUpdujnJIk0RHwLhxFWh66mC9gvg130_provenance.