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Details on Person Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
| Class:Id | LiteratureReference:5625705 |
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| _displayName | Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter |
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| _timestamp | 2014-10-06 14:34:36 |
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| author | [Person:5625657] Nezu, J
[Person:5625716] Tamai, I
[Person:5625699] Oku, A
[Person:5625681] Ohashi, R
[Person:5625655] Yabuuchi, H
[Person:5625652] Hashimoto, N
[Person:5625613] Nikaido, H
[Person:5625695] Sai, Y
[Person:5625687] Koizumi, A
[Person:5625649] Shoji, Y
[Person:5625676] Takada, G
[Person:5625638] Matsuishi, T
[Person:5625641] Yoshino, M
[Person:2317406] Kato, H
[Person:5625642] Ohura, T
[Person:5625659] Tsujimoto, G
[Person:5625701] Hayakawa, J
[Person:5625670] Shimane, M
[Person:2458284] Tsuji, A |
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| created | [InstanceEdit:5625621] Jassal, Bijay, 2014-10-06 |
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| journal | Nat. Genet. |
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| pages | 91-4 |
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| pubMedIdentifier | 9916797 |
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| title | Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter |
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| volume | 21 |
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| year | 1999 |
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| (literatureReference) | [FailedReaction:5625674] Defective SLC22A5 does not cotransport CAR, Na+ from extracellular region to cytosol [Homo sapiens] |
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