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Details on Person Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia.
| Class:Id | LiteratureReference:70681 |
|---|---|
| _displayName | Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia. |
| _timestamp | 2015-06-17 20:37:57 |
| author | [Person:70682] Geraghty, Michael T [Person:70683] Vaughn, D [Person:70684] Nicholson, A J [Person:70685] Lin, Wei Wen [Person:70686] Jimenez-Sanchez, G [Person:70621] Obie, Cassandra [Person:70687] Flynn, M P [Person:70630] Valle, David [Person:70624] Hu, Chien-an A |
| journal | Hum Mol Genet |
| modified | [InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17 |
| pages | 1411-5 |
| pubMedIdentifier | 9700195 |
| title | Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia. |
| volume | 7 |
| year | 1998 |
| (literatureReference) | [Summation:70680] Mitochondrial delta-1-pyrroline-5-carboxylate dehydrogenase ... [Reaction:70679] ALDH4A1 oxidises L-GluSS to Glu [Homo sapiens] |
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No pathways have been reviewed or authored by Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia. (70681)
