Query author contributions in Reactome
Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.
If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.
Details on Person Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
| Class:Id | LiteratureReference:2995342 |
|---|---|
| _displayName | Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency |
| _timestamp | 2013-01-22 11:17:35 |
| author | [Person:2995323] Bugiani, M [Person:2995327] Tiranti, V [Person:2995325] Farina, L [Person:2995339] Uziel, G [Person:2453726] Zeviani, M |
| created | [InstanceEdit:2995335] Jassal, B, 2013-01-22 |
| journal | J. Med. Genet. |
| pages | e28 |
| pubMedIdentifier | 15863660 |
| title | Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency |
| volume | 42 |
| year | 2005 |
| (literatureReference) | [Reaction:2995334] COX15 transforms heme O to heme A [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency (2995342)
