Query author contributions in Reactome
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Pathways reviewed by Christodoulou, John (5432498)
Details on Person Christodoulou, John
| Class:Id | Person:5432498 |
| _displayName | Christodoulou, John |
| _timestamp | 2019-08-16 02:57:56 |
| affiliation | [Affiliation:9640592] Murdoch Children's Research Institute |
| created | [InstanceEdit:5432556] May, Bruce, 2014-05-11 |
| crossReference | [DatabaseIdentifier:9658531] ORCID:0000-0002-8431-0641 |
| firstname | John |
| initial | J |
| modified | [InstanceEdit:9640593] Orlic-Milacic, Marija, 2019-04-01 [InstanceEdit:9658533] Orlic-Milacic, Marija, 2019-08-16 |
| surname | Christodoulou |
| (author) | [LiteratureReference:5432420] Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation [LiteratureReference:5638214] Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin [LiteratureReference:9006581] Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype [LiteratureReference:9615846] RettBASE: Rett syndrome database update [URL:9615850] http://mecp2.chw.edu.au/ [LiteratureReference:9831596] Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency [LiteratureReference:9865895] Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression [InstanceEdit:9608114] Christodoulou, John, 2018-08-07 |
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