Query author contributions in Reactome
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Details on Person Lin, Jean-Pierre
| Class:Id | Person:3165239 |
|---|---|
| _displayName | Lin, Jean-Pierre |
| _timestamp | 2013-02-22 16:13:34 |
| created | [InstanceEdit:3165246] Jassal, B, 2013-02-22 |
| firstname | Jean-Pierre |
| initial | JP |
| surname | Lin |
| (author) | [LiteratureReference:3165248] Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54 [LiteratureReference:9823171] KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation |
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No pathways have been reviewed or authored by Lin, Jean-Pierre (3165239)
