Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase
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| Description | scientific article |
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author: Delphine Héron Nathalie Seta Brigitte Bader-Meunier Patrice Codogno Isabelle Chantret |
| Publication date | July 12, 2002 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |