DNA Clues: Diagnosing the Undiagnosed
About this episode
This episode explores how researchers identified variants in the gene ZMYM3 as a potential cause of neurodevelopmental symptoms in children worldwide.
When more than 20 children worldwide developed similar neurodevelopmental symptoms, scientists turned to DNA for answers. In this episode, we explore how researchers used innovative genetic tools—and a little matchmaking—to identify variants in the gene ZMYM3 as a potential cause. Go behind the scenes in the lab to see how science is ending diagnostic odysseys for families around the world. To go behind the scenes and learn more about this episode, visit "DNA Clues: Diagnosing the Undiagnose...
More episodes of Tiny Expeditions - A Podcast about Genetics, DNA and Inheritance
- The Wiregrass Peanut Revolution
- From Lifespan to Healthspan: Rethinking Brain Wellness
- Beyond the Headlines: How Biomarkers and Genetics Are Changing Neurodegenerative Disease Research
- Turning Pain Into Purpose: Advocating for Families with Rett Syndrome
- Brain Health: What happens when things go wrong?
- Tiny Expeditions Season 6 Promo
Explore listener stats, chart rankings, contacts and more on the Tiny Expeditions - A Podcast about Genetics, DNA and Inheritance podcast page.