Query author contributions in Reactome
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Details on Person Mowat, David
| Class:Id | Person:8877980 |
|---|---|
| _displayName | Mowat, David |
| _timestamp | 2016-06-28 21:29:15 |
| created | [InstanceEdit:8877966] Rothfels, Karen, 2016-06-28 |
| firstname | David |
| initial | D |
| surname | Mowat |
| (author) | [LiteratureReference:8877974] Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome [LiteratureReference:9023252] Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity [LiteratureReference:9765342] ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome |
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No pathways have been reviewed or authored by Mowat, David (8877980)
