Scientists probe genetic roots of devastating childhood illnesses

NCT ID NCT05514470

Summary

This study aimed to understand how specific genetic mutations cause rare and severe diseases that affect multiple organs in children, including the lungs, liver, and brain. Researchers planned to study skin cells from patients in a lab to see how these mutations disrupt the cell's ability to make proteins. The goal was to gather basic knowledge about these poorly understood diseases, but the study was withdrawn before any participants were enrolled.

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Contacts and locations

Locations

  • Hôpital Necker-Enfants Malades

    Paris, 75015, France

Conditions

Explore the condition pages connected to this study.