Query author contributions in Reactome

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Details on Person Murayama, Kei

Class:Id	Person:8855041
_displayName	Murayama, Kei
_timestamp	2016-01-30 19:13:01
created	[InstanceEdit:8855056] D'Eustachio, Peter, 2016-01-30
firstname	Kei
initial	K
modified	[InstanceEdit:8855061] D'Eustachio, Peter, 2016-01-30
surname	Murayama
(author)	[LiteratureReference:8855039] Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26 [LiteratureReference:9672910] Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion [LiteratureReference:9676139] Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease [LiteratureReference:9865701] Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and Neurogenesis [LiteratureReference:9916599] A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies [LiteratureReference:9916618] Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
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No pathways have been reviewed or authored by Murayama, Kei (8855041)