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Researchers Identify Ultra-Rare Genetic Disorder in Amish Communities

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Manage episode 505522724 series 2661438
Content provided by WITF. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by WITF or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

A collaborative study by the Clinic for Special Children in Lancaster and the Children’s Hospital of Philadelphia has identified an ultra-rare genetic disorder called complement factor I (CFI) deficiency, which is significantly more prevalent in individuals of Old Order Amish ancestry.

Support WITF: https://www.witf.org/support/give-now/

See omnystudio.com/listener for privacy information.

  continue reading

110 episodes

Artwork
iconShare
 
Manage episode 505522724 series 2661438
Content provided by WITF. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by WITF or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

A collaborative study by the Clinic for Special Children in Lancaster and the Children’s Hospital of Philadelphia has identified an ultra-rare genetic disorder called complement factor I (CFI) deficiency, which is significantly more prevalent in individuals of Old Order Amish ancestry.

Support WITF: https://www.witf.org/support/give-now/

See omnystudio.com/listener for privacy information.

  continue reading

110 episodes

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