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Ferroportin mutations: a tale of two phenotypes
| Content Provider | Scilit |
|---|---|
| Author | Nemeth, Elizabeta |
| Copyright Year | 2005 |
| Description | Comment on Schimanski et al, page [4096][1] Ferroportin disease is becoming recognized as the most common form of hereditary iron overload after HFE hemochromatosis, but explanations for its autosomal dominant inheritance and heterogeneous clinical presentation have been elusive. Schimanski and |
| Related Links | http://www.bloodjournal.org/content/bloodjournal/105/10/3763.full.pdf |
| Ending Page | 3764 |
| Page Count | 2 |
| Starting Page | 3763 |
| DOI | 10.1182/blood-2005-02-0771 |
| Journal | Blood |
| Issue Number | 10 |
| Volume Number | 105 |
| Language | English |
| Publisher | American Society of Hematology |
| Publisher Date | 2005-05-15 |
| Access Restriction | Open |
| Subject Keyword | Urology and Nephrology Ferroportin Mutations Tale of Two Phenotypes Journal: Blood (Vol- 113, Issue- 10) |
| Content Type | Text |
| Resource Type | Article |