Publication
| Schenk B, Imbach T, Frank CG, Grubenmann CE, Raymond GV, Hurvitz H, Korn-Lubetzki I, Revel-Vik S, Raas-Rotschild A, Luder AS, Jaeken J, Berger EG, Matthijs G, Hennet T, Aebi M, MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If The Journal of clinical investigation108:1687-95 2001 |
| PubMed ID: 11733564 |
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| Records Return:
(1)
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| Catalog ID | Gender | Description | Collection_Type_id |
| GM20958 | Male | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If | GM |
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