Query author contributions in Reactome
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Details on Person Auray-Blais, Christiane
| Class:Id | Person:5625031 |
|---|---|
| _displayName | Auray-Blais, Christiane |
| _timestamp | 2014-10-01 12:43:54 |
| created | [InstanceEdit:5625030] Jassal, Bijay, 2014-10-01 |
| firstname | Christiane |
| initial | C |
| surname | Auray-Blais |
| (author) | [LiteratureReference:5625009] Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria [LiteratureReference:5653856] Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters [LiteratureReference:6797948] Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia |
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No pathways have been reviewed or authored by Auray-Blais, Christiane (5625031)
