Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter
| author | |
| created | [InstanceEdit:735694] Jassal, Bijay, 2010-05-13 |
| dbId | 735687 |
| displayName | Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter |
| journal | Blood |
| pages | 2671-6 |
| pubMedIdentifier | 15576474 |
| schemaClass | LiteratureReference |
| title | Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter |
| url | http://www.ncbi.nlm.nih.gov/pubmed/15576474 |
| volume | 105 |
| year | 2005 |
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