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Polymorphisms and Mutations of Human TMPRSS6 in Iron Deficiency Anemia
Male subjects with iron deficiency from the general population were examined for polymorphisms or sporadic mutations in TMPRSS6 to identify genetic risk factors for iron deficiency anemia. Three uncommon non-synonymous polymorphisms were identified, G228D, R446W, and V795I (allele frequencies 0.0074...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2818284/ https://ncbi.nlm.nih.gov/pubmed/19818657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bcmd.2009.09.001 |
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