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Details on Person Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy
| Class:Id | LiteratureReference:5661438 |
|---|---|
| _displayName | Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy |
| _timestamp | 2015-01-12 14:44:45 |
| author | [Person:5661420] Zhang, Zhenlin [Person:5602145] Xia, Weibo [Person:5661433] He, Jinwei [Person:5661412] Zhang, Zeng [Person:5661405] Ke, Yaohua [Person:5661429] Yue, Hua [Person:5661469] Wang, Chun [Person:5661472] Zhang, Hao [Person:5661424] Gu, Jiemei [Person:5661476] Hu, Weiwei [Person:5661459] Fu, Wenzhen [Person:5661427] Hu, Yunqiu [Person:5661419] Li, Miao [Person:5661385] Liu, Yujuan |
| created | [InstanceEdit:5661406] Jassal, Bijay, 2015-01-12 |
| journal | Am. J. Hum. Genet. |
| pages | 125-32 |
| pubMedIdentifier | 22197487 |
| title | Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy |
| volume | 90 |
| year | 2012 |
| (literatureReference) | [FailedReaction:5661188] Defective SLCO2A1 does not transport PGT substrates from extracellular region to cytosol [Homo sapiens] |
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No pathways have been reviewed or authored by Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy (5661438)
