Diseases, Conditions, Syndromes
Spanish scientists identify the key cell type for strategies to prevent atherosclerosis in progeria syndrome
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disease that affects just 1 in every 20 million people; it is estimated that fewer than 400 children in the world have the disease. HGPS is characterized ...
Apr 22, 2024
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