Reactome | Cavanaugh, JA

Schema > Person > Entries

created	[InstanceEdit:198855] D'Eustachio, P, 2007-07-05 13:28:49
dbId	198785
displayName	Cavanaugh, JA
firstname	Juleen A
initial	JA
publications	[LiteratureReference:198859] Characterization of the monomethylarsonate reductase and dehydroascorbate reductase activities of Omega class glutathione transferase variants: implications for arsenic metabolism and the age-at-onset of Alzheimer's and Parkinson's diseases [LiteratureReference:375453] Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19 [LiteratureReference:5653856] Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters
schemaClass	Person
surname	Cavanaugh

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