https://www.ncbi.nlm.nih.gov/gene/4891
SLC11A2 solute carrier family 11 member 2 [Homo sapiens (human)] - Gene - NCBI
carrier family
https://pubmed.ncbi.nlm.nih.gov/21871825/
A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association...
Our data confirm the major role of DMT1 in the maintenance of iron homeostasis in humans and demonstrate that the N491S mutation, through its deleterious...
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035015
Candidate Gene Sequencing of SLC11A2 and TMPRSS6 in a Family with Severe Anaemia: Common SNPs, Rare...
Background Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which was linked to mutations in two genes (SLC11A2 and TMPRSS6). Common...