Pub. Date : 2014 Sep 1
PMID : 24714983
4 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Hemochromatosis type 4 is a rare form of primary iron overload transmitted as an autosomal dominant trait caused by mutations in the gene encoding the iron transport protein ferroportin 1 (SLC40A1). | Iron | solute carrier family 40 member 1 | Homo sapiens |
| 2 | Hemochromatosis type 4 is a rare form of primary iron overload transmitted as an autosomal dominant trait caused by mutations in the gene encoding the iron transport protein ferroportin 1 (SLC40A1). | Iron | solute carrier family 40 member 1 | Homo sapiens |
| 3 | Hemochromatosis type 4 is a rare form of primary iron overload transmitted as an autosomal dominant trait caused by mutations in the gene encoding the iron transport protein ferroportin 1 (SLC40A1). | Iron | solute carrier family 40 member 1 | Homo sapiens |
| 4 | Hemochromatosis type 4 is a rare form of primary iron overload transmitted as an autosomal dominant trait caused by mutations in the gene encoding the iron transport protein ferroportin 1 (SLC40A1). | Iron | solute carrier family 40 member 1 | Homo sapiens |