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Details on Person Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment
| Class:Id | LiteratureReference:3165233 |
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| _displayName | Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment |
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| _timestamp | 2015-11-12 17:26:39 |
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| author | [Person:3165250] Bosch, Annet M
[Person:5320946] Abeling, Nico G G M
[Person:70777] Ijlst, L
[Person:3165251] Knoester, Hennie
[Person:3165252] van der Pol, W Ludo
[Person:5320944] Stroomer, Alida E M
[Person:201079] Wanders, Ronald J A
[Person:375464] Visser, G
[Person:3165249] Wijburg, Frits A
[Person:70780] Duran, M
[Person:191298] Waterham, HR |
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| created | [InstanceEdit:3165246] Jassal, B, 2013-02-22 |
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| journal | J. Inherit. Metab. Dis. |
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| modified | [InstanceEdit:5364054] D'Eustachio, Peter, 2014-04-19
[InstanceEdit:6809722] D'Eustachio, Peter, 2015-11-12 |
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| pages | 159-64 |
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| pubMedIdentifier | 21110228 |
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| title | Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment |
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| volume | 34 |
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| year | 2011 |
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| (literatureReference) | [Reaction:3165230] SLC52A1,2,3 transport RIB from extracellular region to cytosol [Homo sapiens] |
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