| Autor: |
van Rooijen KL; Universitair Medisch Centrum St. Radboud, Afd. Hematologie, Nijmegen, the Netherlands., Raymakers RA, Cuijpers ML, Brons PP, Janssen MC, Swinkels DW |
| Jazyk: |
Dutch; Flemish |
| Zdroj: |
Nederlands tijdschrift voor geneeskunde [Ned Tijdschr Geneeskd] 2010; Vol. 154, pp. A1039. |
| Abstrakt: |
Recently various new gene defects have been identified which explain some previously unknown causes of inherited microcytic anaemias. These defects are located in genes that encode for the cellular iron importing protein Divalent Metal Transporter 1 (DMT1), the iron exporting protein ferroportin, the mitochondrial enzyme glutaredoxin-5 and the hepatocyte membrane protein matriptase-2. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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