Query author contributions in Reactome

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Details on Person Lin, Wei Wen

Class:Id	Person:70685
_displayName	Lin, Wei Wen
_timestamp	2015-06-17 20:37:54
firstname	Wei Wen
initial	WW
modified	[InstanceEdit:508032] D'Eustachio, P, 2010-02-10 [InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17
surname	Lin
(author)	[LiteratureReference:70681] Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia. [LiteratureReference:508038] Molecular enzymology of mammalian Delta1-pyrroline-5-carboxylate synthase. Alternative splice donor utilization generates isoforms with different sensitivity to ornithine inhibition [LiteratureReference:517457] Cloning, characterization, and expression of cDNAs encoding human delta 1-pyrroline-5-carboxylate dehydrogenase [LiteratureReference:517459] Functional consequences of PRODH missense mutations
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No pathways have been reviewed or authored by Lin, Wei Wen (70685)