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L’hémochromatose génétique est dans la majorité des cas principalement due à la mutation p.Cys282Tyr du gène HFE, mais d’autres gènes peuvent être impliqués. Les progrès dans la connaissance du métabolisme du fer ont permis de mettre en évidence le rôle central de l’hepcidine. Les manifestations ostéoarticulaires de la maladie sont au premier plan tant au moment du diagnostic qu’à la phase d’état...
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.