A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.

Source:http://linkedlifedata.com/resource/pubmed/id/20080937

Hum. Mol. Genet. 2010 Apr 15 19 8 1413-24

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PMID
20080937