Carregant...
Ferroportin disease mutations influence manganese accumulation and cytotoxicity
Hemochromatosis is a frequent genetic disorder, characterized by the accumulation of excess iron across tissues. Mutations in the FPN1 gene, encoding a cell surface iron exporter [ferroportin (Fpn)], are responsible for hemochromatosis type 4, also known as ferroportin disease. Recently, Fpn has bee...
Guardat en:
| Publicat a: | FASEB J |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Federation of American Societies for Experimental Biology
2019
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6338638/ https://ncbi.nlm.nih.gov/pubmed/30247984 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.201800831R |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|