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Details on Person Hereditary inclusion body myopathy: the Middle Eastern genetic cluster

Class:IdLiteratureReference:4088349
_displayNameHereditary inclusion body myopathy: the Middle Eastern genetic cluster
_timestamp2013-08-13 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
journalNeurology
pages1519-23
pubMedIdentifier12743242
titleHereditary inclusion body myopathy: the Middle Eastern genetic cluster
volume60
year2003
(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)