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Details on Person Hereditary inclusion body myopathy: the Middle Eastern genetic cluster
| Class:Id | LiteratureReference:4088349 |
|---|---|
| _displayName | Hereditary inclusion body myopathy: the Middle Eastern genetic cluster |
| _timestamp | 2013-08-13 13:13:42 |
| author | [Person:4085216] Argov, Z [Person:4085201] Eisenberg, I [Person:4085218] Grabov-Nardini, G [Person:4085243] Sadeh, M [Person:4088336] Wirguin, I [Person:4088389] Soffer, D [Person:4085189] Mitrani-Rosenbaum, S |
| created | [InstanceEdit:4088407] Jassal, B, 2013-08-13 |
| journal | Neurology |
| pages | 1519-23 |
| pubMedIdentifier | 12743242 |
| title | Hereditary inclusion body myopathy: the Middle Eastern genetic cluster |
| volume | 60 |
| year | 2003 |
| (literatureReference) | [Reaction:4085021] GNE hydrolyzes and epimerises UDP-GlcNAc to ManNAc and UDP [Homo sapiens] [Reaction:4085028] GNE phosphorylates ManNAc to ManNAc-6-P [Homo sapiens] [FailedReaction:4088322] Defective GNE does not phosphorylate ManNAc to ManNAc-6-P [Homo sapiens] [FailedReaction:4088338] Defective GNE does not hydrolyse UDP-GlcNAc [Homo sapiens] |
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No pathways have been reviewed or authored by Hereditary inclusion body myopathy: the Middle Eastern genetic cluster (4088349)
