3 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
| 1 | 29270100 | Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes. | 2017 | 1 |
| 2 | 16462140 | New aspects of copper and iron metabolism in the myelodysplastic syndromes. | 2006 | 2 |
| 3 | 16998622 | Compound overload of copper and iron in patients with Wilson's disease. | 2006 Sep | 1 |