Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl Mannosyltransferase
Open Access
- 1 July 2002
- journal article
- Published by Elsevier
- Vol. 277 (28), 25815-25822
- https://doi.org/10.1074/jbc.m203285200
Abstract
No abstract availableKeywords
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