Scientists hunt for missing genetic clues in rare anemia
NCT ID NCT07459816
Summary
This study aims to discover the unknown genetic causes of congenital sideroblastic anemia, a rare disorder where the body struggles to make healthy red blood cells. Researchers will analyze the complete genetic code of 20 patients whose condition has no known genetic explanation. The goal is to identify new gene mutations responsible for the disease to improve future diagnosis and understanding.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Amiens University Hospital
RECRUITINGAmiens, 80054, France
Conditions
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