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Details on Person Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin
| Class:Id | LiteratureReference:3000253 |
|---|---|
| _displayName | Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin |
| _timestamp | 2021-11-24 15:03:10 |
| author | [Person:3000269] Kristiansen, M [Person:3000271] Aminoff, M [Person:3000235] Jacobsen, C [Person:3000266] de la Chapelle, A [Person:3000248] Krahe, R [Person:3000240] Verroust, Pierre J [Person:2512876] Moestrup, Søren Kragh |
| created | [InstanceEdit:3000234] Jassal, Bijay, 2013-01-24 |
| journal | Blood |
| modified | [InstanceEdit:9758689] D'Eustachio, Peter, 2021-11-24 |
| pages | 405-9 |
| pubMedIdentifier | 10887099 |
| title | Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin |
| volume | 96 |
| year | 2000 |
| (literatureReference) | [Reaction:3000103] CUBN:AMN binds CBLIF:RCbl [Homo sapiens] [FailedReaction:3296462] Defective CUBN does not transport GIF:Cbl [Homo sapiens] |
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No pathways have been reviewed or authored by Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin (3000253)
