Nieuwe oorzaken van microcytaire anemie: erfelijke stoornissen in de ijzerhomeostase

Karlijn L van Rooijen; Reinier A P Raymakers; Marloes L H Cuijpers; Paul P T Brons; Mirian C H Janssen; Dorine W Swinkels

Nieuwe oorzaken van microcytaire anemie: erfelijke stoornissen in de ijzerhomeostase

Translated title of the contribution: New causes of microcytic anaemia: hereditary disorders of iron homeostasis

Karlijn L van Rooijen, Reinier A P Raymakers, Marloes L H Cuijpers, Paul P T Brons, Mirian C H Janssen, Dorine W Swinkels

Research output: Contribution to journal › Review article › peer-review

Abstract

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.

Translated title of the contribution	New causes of microcytic anaemia: hereditary disorders of iron homeostasis
Original language	Dutch
Pages (from-to)	A1039
Journal	Nederlands tijdschrift voor geneeskunde
Volume	154
Publication status	Published - 2010

Keywords

Anemia
Cation Transport Proteins
Genetic Diseases, Inborn
Glutaredoxins
Homeostasis
Humans
Iron
Membrane Proteins
Serine Endopeptidases
English Abstract
Journal Article
Review

Cite this

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title = "Nieuwe oorzaken van microcytaire anemie: erfelijke stoornissen in de ijzerhomeostase",

abstract = "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.",

keywords = "Anemia, Cation Transport Proteins, Genetic Diseases, Inborn, Glutaredoxins, Homeostasis, Humans, Iron, Membrane Proteins, Serine Endopeptidases, English Abstract, Journal Article, Review",

author = "{van Rooijen}, {Karlijn L} and Raymakers, {Reinier A P} and Cuijpers, {Marloes L H} and Brons, {Paul P T} and Janssen, {Mirian C H} and Swinkels, {Dorine W}",

year = "2010",

language = "Dutch",

volume = "154",

pages = "A1039",

journal = "Nederlands tijdschrift voor geneeskunde",

issn = "0028-2162",

publisher = "Bohn Stafleu van Loghum",

}

TY - JOUR

T1 - Nieuwe oorzaken van microcytaire anemie

T2 - erfelijke stoornissen in de ijzerhomeostase

AU - van Rooijen, Karlijn L

AU - Raymakers, Reinier A P

AU - Cuijpers, Marloes L H

AU - Brons, Paul P T

AU - Janssen, Mirian C H

AU - Swinkels, Dorine W

PY - 2010

Y1 - 2010

N2 - 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.

AB - 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.

KW - Anemia

KW - Cation Transport Proteins

KW - Genetic Diseases, Inborn

KW - Glutaredoxins

KW - Homeostasis

KW - Humans

KW - Iron

KW - Membrane Proteins

KW - Serine Endopeptidases

KW - English Abstract

KW - Journal Article

KW - Review

M3 - Review article

C2 - 20619018

SN - 0028-2162

VL - 154

SP - A1039

JO - Nederlands tijdschrift voor geneeskunde

JF - Nederlands tijdschrift voor geneeskunde

ER -

Nieuwe oorzaken van microcytaire anemie: erfelijke stoornissen in de ijzerhomeostase

Abstract

Keywords

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