Scientists hunt for genetic clues to mysterious childhood disorder
NCT ID NCT02866162
Summary
This study aimed to discover the genetic causes of a rare disorder where children are born with very low white blood cells and other developmental differences. Researchers analyzed the genes of 25 participants with this condition to find the specific genes responsible. The goal was to improve understanding, not to test a treatment.
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Contacts and locations
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Locations
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CHU Dijon Bourgogne
Dijon, 21079, France
Conditions
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