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Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia
BACKGROUND: Congenital sideroblastic anemias are rare disorders with several genetic causes; they are characterized by erythroblast mitochondrial iron overload, differ greatly in severity and some occur within a syndrome. The most common cause of non-syndromic, microcytic sideroblastic anemia is a d...
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| Main Authors: | , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3105641/ https://ncbi.nlm.nih.gov/pubmed/21393332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2010.039164 |
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