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International News
- Gene editing technology shines light on rare dyskeratosis congenitaUsing the gene editing technology CRISPR, scientists have shed light on a rare, sometimes fatal syndrome that causes children to gradually lose the ability to manufacture vital blood cells. […]
- Researchers detect new gene mutation linked to Fanconi anemiaFanconi anemia is a rare genetic disease characterized by bone marrow failure heralded by low platelet counts and unusually large red blood cells. […]
