A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip
| author | |
| created | [InstanceEdit:5615515] Jassal, Bijay, 2014-07-24 |
| dbId | 5615516 |
| displayName | A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip |
| journal | Hum. Mol. Genet. |
| pages | 1413-24 |
| pubMedIdentifier | 20080937 |
| schemaClass | LiteratureReference |
| title | A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip |
| url | http://www.ncbi.nlm.nih.gov/pubmed/20080937 |
| volume | 19 |
| year | 2010 |
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