Query author contributions in Reactome

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Details on Person Trembath, Richard C

Class:Id	Person:3322906
_displayName	Trembath, Richard C
_timestamp	2013-05-06 15:44:22
created	[InstanceEdit:3322896] Orlic-Milacic, M, 2013-05-06
firstname	Richard C
initial	RC
surname	Trembath
(author)	[LiteratureReference:3322899] Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss [LiteratureReference:5628748] Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease [LiteratureReference:8858381] Bone morphogenetic protein (BMP) and activin type II receptors balance BMP9 signals mediated by activin receptor-like kinase-1 in human pulmonary artery endothelial cells [LiteratureReference:8941492] Mutations in IL36RN/IL1F5 are associated with the severe episodic inflammatory skin disease known as generalized pustular psoriasis
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No pathways have been reviewed or authored by Trembath, Richard C (3322906)