Query author contributions in Reactome
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Details on Person Pfundt, Rolph
| Class:Id | Person:5623726 |
|---|---|
| _displayName | Pfundt, Rolph |
| _timestamp | 2014-09-19 08:45:41 |
| created | [InstanceEdit:5623756] Jassal, Bijay, 2014-09-19 |
| firstname | Rolph |
| initial | R |
| surname | Pfundt |
| (author) | [LiteratureReference:5623692] Novel NCC mutants and functional analysis in a new cohort of patients with Gitelman syndrome [LiteratureReference:5661029] Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing [LiteratureReference:9823180] Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome |
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No pathways have been reviewed or authored by Pfundt, Rolph (5623726)
