Query author contributions in Reactome

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Details on Person Rosenblatt, DS

Class:Id	Person:71003
_displayName	Rosenblatt, DS
_timestamp	0000-00-00 00:00:00
firstname	David S
initial	DS
surname	Rosenblatt
(author)	[LiteratureReference:200714] Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency [LiteratureReference:200732] Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders [LiteratureReference:517423] The molecular basis of glutamate formiminotransferase deficiency [LiteratureReference:3000076] Positive newborn screen for methylmalonic aciduria identifies the first mutation in TCblR/CD320, the gene for cellular uptake of transcobalamin-bound vitamin B(12) [LiteratureReference:3000283] Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism [LiteratureReference:3095895] Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type [LiteratureReference:3132779] Inborn errors of cobalamin absorption and metabolism [LiteratureReference:3149487] Interaction between MMACHC and MMADHC, two human proteins participating in intracellular vitamin B?? metabolism [LiteratureReference:3149507] Processing of alkylcobalamins in mammalian cells: A role for the MMACHC (cblC) gene product [LiteratureReference:3149523] Structural features of recombinant MMADHC isoforms and their interactions with MMACHC, proteins of mammalian vitamin B12 metabolism List all 24 refering instances
(chapterAuthors)	[Book:71000] The Metabolic and Molecular Bases of Inherited Disease, 8th ed Scriver, CR Disorders of propionate and methylmalonate metabolism 0079130356
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No pathways have been reviewed or authored by Rosenblatt, DS (71003)