[New causes of microcytic anaemia: hereditary disorders of iron homeostasis]

Autor: Karlijn L, van Rooijen, Reinier A P, Raymakers, Marloes L H, Cuijpers, Paul P T, Brons, Mirian C H, Janssen, Dorine W, Swinkels
Jazyk: Dutch; Flemish
Rok vydání: 2010
Předmět:
Zdroj: Nederlands tijdschrift voor geneeskunde. 154
ISSN: 1876-8784
Popis: 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: OpenAIRE