Query author contributions in Reactome
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Details on Person Brendel, Cornelia
| Class:Id | Person:5638268 |
|---|---|
| _displayName | Brendel, Cornelia |
| _timestamp | 2014-11-13 15:46:24 |
| created | [InstanceEdit:5638236] Jassal, Bijay, 2014-11-13 |
| firstname | Cornelia |
| initial | C |
| surname | Brendel |
| (author) | [LiteratureReference:5638214] Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin |
| [Change default viewing format] | |
No pathways have been reviewed or authored by Brendel, Cornelia (5638268)
