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Details on Person Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs
| Class:Id | LiteratureReference:3700920 |
|---|---|
| _displayName | Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs |
| _timestamp | 2013-06-11 12:43:16 |
| author | [Person:3700874] Sandhoff, K [Person:3700891] Andreae, U [Person:3700946] Jatzkewitz, H |
| created | [InstanceEdit:3700835] Jassal, B, 2013-06-11 |
| journal | Life Sci. |
| pages | 283-8 |
| pubMedIdentifier | 5651108 |
| title | Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs |
| volume | 7 |
| year | 1968 |
| (literatureReference) | [Pathway:3656248] Defective HEXB causes GM2G2 (Hyaluronan metabolism) [Homo sapiens] [Pathway:9953282] Defective HEXB causes GM2G2 (CS/DS degradation) [Homo sapiens] [Pathway:9953284] Defective HEXB causes GM2G2 (Keratan metabolism) [Homo sapiens] |
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No pathways have been reviewed or authored by Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs (3700920)
