Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
about
Iron deficiency anemia: a common and curable diseaseThe conundrum of iron in multiple sclerosis--time for an individualised approach.Diagnosis of anaemia: old things rearranged.Nomograms incorporating genetic variants in BMP/Smad4/Hamp pathway to predict disease outcomes after definitive radiotherapy for non-small cell lung cancer.
P2860
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
@en
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
@nl
type
label
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
@en
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
@nl
prefLabel
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
@en
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
@nl
P2093
P2860
P356
P1476
Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.
@en
P2093
Maria Antonietta Melis
Milena Cau
Renzo Galanello
Rita Congiu
P2860
P304
P356
10.1586/EHM.10.2
P577
2010-04-01T00:00:00Z