Query author contributions in Reactome

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Details on Person Thorburn, David R

Class:Id	Person:5432452
_displayName	Thorburn, David R
_timestamp	2014-05-11 03:21:23
created	[InstanceEdit:5432556] May, Bruce, 2014-05-11
firstname	David R
initial	DR
surname	Thorburn
(author)	[LiteratureReference:5432420] Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation [LiteratureReference:6788511] Understanding mitochondrial complex I assembly in health and disease [LiteratureReference:9865685] HIGD2A is Required for Assembly of the COX3 Module of Human Mitochondrial Complex IV [LiteratureReference:9865895] Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression [LiteratureReference:9906620] Accessory subunits are integral for assembly and function of human mitochondrial complex I [LiteratureReference:9906635] Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I [LiteratureReference:9906974] Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module [LiteratureReference:9916885] Mutations in the gene encoding 3-hydroxyisobutyryl-CoA hydrolase results in progressive infantile neurodegeneration
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No pathways have been reviewed or authored by Thorburn, David R (5432452)