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Details on Person Molecular basis of an adult form of beta-hexosaminidase B deficiency with motor neuron disease
| Class:Id | LiteratureReference:1605668 |
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| _displayName | Molecular basis of an adult form of beta-hexosaminidase B deficiency with motor neuron disease |
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| _timestamp | 2011-09-21 09:55:12 |
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| author | [Person:1605678] Banerjee, P
[Person:1605599] Siciliano, L
[Person:1605757] Oliveri, D
[Person:1605689] McCabe, NR
[Person:1605622] Boyers, MJ
[Person:1605659] Horwitz, AL
[Person:1605785] Li, SC
[Person:1605800] Dawson, G |
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| created | [InstanceEdit:1605804] Jassal, Bijay, 2011-09-21 |
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| journal | Biochem Biophys Res Commun |
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| modified | [InstanceEdit:1605814] Jassal, B, 2011-09-21 |
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| pages | 108-15 |
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| pubMedIdentifier | 1720305 |
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| title | Molecular basis of an adult form of beta-hexosaminidase B deficiency with motor neuron disease |
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| volume | 181 |
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| year | 1991 |
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| (literatureReference) | [Reaction:1605595] bHEXA hydrolyzes GM2A:GM2 to GM2A:GM3 [Homo sapiens]
[Pathway:3656248] Defective HEXB causes GM2G2 (Hyaluronan metabolism) [Homo sapiens]
[FailedReaction:3662344] Defective HEXB does not cleave the terminal GalNAc from DS [Homo sapiens]
[FailedReaction:9035982] Defective HEXB does not cleave the terminal GalNAc from HA fragments [Homo sapiens]
[FailedReaction:9035983] Defective HEXB does not cleave the terminal GalNAc from keratan sulfate [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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