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Details on Person Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism
| Class:Id | LiteratureReference:3149477 |
|---|---|
| _displayName | Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism |
| _timestamp | 2013-02-15 15:21:59 |
| author | [Person:2672403] Wilson, A [Person:200677] Leclerc, D [Person:3149522] Rosenblatt, David [Person:3149549] Gravel, R A |
| created | [InstanceEdit:3149501] Jassal, Bijay, 2013-02-15 |
| journal | Hum. Mol. Genet. |
| pages | 2009-16 |
| pubMedIdentifier | 10484769 |
| title | Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism |
| volume | 8 |
| year | 1999 |
| (literatureReference) | [Reaction:3149518] MTRR reduces cob(II)alamin to meCbl [Homo sapiens] [FailedReaction:3318563] Defective MTRR does not convert cob(II)alamin to MeCbl [Homo sapiens] [Pathway:3359467] Defective MTRR causes HMAE [Homo sapiens] |
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No pathways have been reviewed or authored by Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism (3149477)
