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Details on Person Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency
| Class:Id | LiteratureReference:549253 |
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| _displayName | Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency |
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| _timestamp | 2015-11-12 17:26:41 |
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| author | [Person:549280] Tang, NL
[Person:549244] Ganapathy, V
[Person:174760] Wu, X
[Person:549286] Hui, J
[Person:549259] Seth, P
[Person:549226] Yuen, PM
[Person:201079] Wanders, Ronald J A
[Person:549256] Fok, TF
[Person:549229] Hjelm, NM |
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| created | [InstanceEdit:549249] Jassal, Bijay, 2010-03-19 |
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| journal | Hum Mol Genet |
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| modified | [InstanceEdit:6809722] D'Eustachio, Peter, 2015-11-12 |
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| pages | 655-60 |
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| pubMedIdentifier | 10072434 |
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| title | Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency |
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| volume | 8 |
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| year | 1999 |
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| (literatureReference) | [Reaction:549297] SLC22A4, 5,15,16 cotransport CAR, Na+ from extracellular region to cytosol [Homo sapiens]
[FailedReaction:5625674] Defective SLC22A5 does not cotransport CAR, Na+ from extracellular region to cytosol [Homo sapiens] |
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