Query author contributions in Reactome

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Details on Person Mitchell, Grant A

Class:Id	Person:70629
_displayName	Mitchell, Grant A
_timestamp	2015-06-17 20:37:56
firstname	Grant A
initial	GA
modified	[InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17
surname	Mitchell
(author)	[LiteratureReference:70619] Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter [LiteratureReference:70640] Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences. [LiteratureReference:200206] Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient [LiteratureReference:200255] 3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency. [LiteratureReference:9915309] Kinetic and expression analyses of seven novel mutations in mitochondrial acetoacetyl-CoA thiolase (T2): identification of a Km mutant and an analysis of the mutational sites in the structure [LiteratureReference:9916626] Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome
(chapterAuthors)	[Book:71156] The Metabolic and Molecular Bases of Inherited Disease, 8th ed Scriver, CR Hypertyrosinemia 0079130356
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No pathways have been reviewed or authored by Mitchell, Grant A (70629)