Ferroportin mutation in autosomal dominant hemochromatosis: loss of function, gain in understanding
about
Recent advances in understanding haemochromatosis: a transition stateIntracellular iron transport and storage: from molecular mechanisms to health implications.Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4.Heme and iron metabolism: role in cerebral hemorrhage.Ferroportin/IREG-1/MTP-1/SLC40A1 modulates the uptake of iron at the apical membrane of enterocytes.Hepcidin in iron overload disordersThe molecular genetics of haemochromatosis.Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.
P2860
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P2860
Ferroportin mutation in autosomal dominant hemochromatosis: loss of function, gain in understanding
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
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2001年學術文章
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2001年學術文章
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name
Ferroportin mutation in autoso ...... unction, gain in understanding
@en
Ferroportin mutation in autoso ...... nction, gain in understanding.
@nl
type
label
Ferroportin mutation in autoso ...... unction, gain in understanding
@en
Ferroportin mutation in autoso ...... nction, gain in understanding.
@nl
prefLabel
Ferroportin mutation in autoso ...... unction, gain in understanding
@en
Ferroportin mutation in autoso ...... nction, gain in understanding.
@nl
P2860
P356
P1476
Ferroportin mutation in autoso ...... unction, gain in understanding
@en
P2093
P2860
P304
P356
10.1172/JCI13739
P407
P577
2001-08-01T00:00:00Z