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Details on Person Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase
| Class:Id | LiteratureReference:449352 |
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| _displayName | Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase |
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| _timestamp | 2009-12-02 13:29:35 |
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| author | [Person:449360] Chantret, I
[Person:449368] Dupré, T
[Person:449358] Delenda, C
[Person:449366] Bucher, S
[Person:449350] Dancourt, J
[Person:449353] Barnier, A
[Person:449351] Charollais, A
[Person:449354] Heron, D
[Person:449363] Bader-Meunier, B
[Person:449361] Danos, O
[Person:449362] Seta, N
[Person:449357] Durand, G
[Person:449359] Oriol, R
[Person:449356] Codogno, P
[Person:191434] Moore, SE |
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| created | [InstanceEdit:449355] Jassal, B, 2009-12-02 |
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| journal | J Biol Chem |
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| pages | 25815-22 |
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| pubMedIdentifier | 11983712 |
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| title | Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase |
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| volume | 277 |
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| year | 2002 |
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| (literatureReference) | [Reaction:446198] ALG12 transfers Man to N-glycan precursor (GlcNAc)2 (Man)7 (PP-Dol)1 [Homo sapiens]
[Pathway:4720489] Defective ALG12 causes CDG-1g [Homo sapiens]
[FailedReaction:4720497] Defective ALG12 does not add mannose to the N-glycan precursor [Homo sapiens] |
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