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Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells
M Priwitzerova, D Pospisilova, JT Prchal, K Indrak, A Hlobilkova, V Mihal, P Ponka, V Divoky
Language English Country United States
Grant support
NM6739
MZ0
CEP Register
Digital library NLK
Full text - Část
Source
NLK
Free Medical Journals
from 1946 to 1 year ago
Freely Accessible Science Journals
from 1946 to 1 year ago
Open Access Digital Library
from 1946-01-01
Open Access Digital Library
from 1946-01-01
ROAD: Directory of Open Access Scholarly Resources
- MeSH
- Adult MeSH
- Erythroblasts cytology chemistry MeSH
- Homozygote MeSH
- Anemia, Hypochromic etiology genetics congenital MeSH
- Humans MeSH
- Cation Transport Proteins genetics deficiency MeSH
- Iron-Binding Proteins genetics MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Female MeSH
Department of Biology Faculty of Medicine Palacky University Olomouc
Department of Hemato oncology Faculty of Medicine Palacky University Olomouc
Department of Medicine Baylor College of Medicine Houston TX USA
Department of Pathology Faculty of Medicine Palacky University Olomouc
Department of Pediatrics Faculty of Medicine Palacky University Olomouc
Literatura
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- $a Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells / $c M Priwitzerova, D Pospisilova, JT Prchal, K Indrak, A Hlobilkova, V Mihal, P Ponka, V Divoky
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- $a Divoký, Vladimír $7 xx0018902 $u Department of Biology, Faculty of Medicine, Palacky University, Olomouc; Department of Hemato-oncology, Faculty of Medicine, Palacky University, Olomouc
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