Query author contributions in Reactome

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Details on Person Rutland, P

Class:Id	Person:1614759
_displayName	Rutland, P
_timestamp	2011-09-29 17:46:28
created	[InstanceEdit:1614758] Rothfels, K, 2011-09-29
firstname	Paul
initial	P
surname	Rutland
(author)	[LiteratureReference:1637876] Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome [LiteratureReference:2023308] A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome [LiteratureReference:2029815] Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome [LiteratureReference:2060840] Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis [LiteratureReference:9906637] FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy
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No pathways have been reviewed or authored by Rutland, P (1614759)