Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload

Class:IdLiteratureReference:5623743
_displayNameIdentification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload
_timestamp2014-09-19 08:45:54
author[Person:5623708] Mims, Martha P
[Person:5623720] Guan, Yongli
[Person:5623745] Pospisilova, Dagmar
[Person:5623766] Priwitzerova, Monika
[Person:5623715] Indrak, Karel
[Person:5623770] Ponka, Prem
[Person:5623734] Divoky, Vladimir
[Person:5623698] Prchal, Josef T
created[InstanceEdit:5623756] Jassal, Bijay, 2014-09-19
journalBlood
pages1337-42
pubMedIdentifier15459009
titleIdentification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload
volume105
year2005
(literatureReference)[FailedReaction:5623558] Defective SLC11A2 does not cotransport Fe2+, H+ from extracellular region to cytosol [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload (5623743)