Query author contributions in Reactome
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Details on Person Loupatty, FJ
| Class:Id | Person:70778 |
|---|---|
| _displayName | Loupatty, FJ |
| _timestamp | 0000-00-00 00:00:00 |
| firstname | Ference J |
| initial | FJ |
| surname | Loupatty |
| (author) | [LiteratureReference:70776] 3-Methylglutaconic aciduria type I is caused by mutations in AUH. [LiteratureReference:9914306] NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism [LiteratureReference:9916885] Mutations in the gene encoding 3-hydroxyisobutyryl-CoA hydrolase results in progressive infantile neurodegeneration |
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No pathways have been reviewed or authored by Loupatty, FJ (70778)
