For a long time, scientists have suspected that stuttering — a common speech condition that affects an estimated 1 in every 100 people — could be heritable. Despite how common it is, it's still a remarkably understudied condition. Geneticists Piper Below and Dillon Pruett were determined to fix that. With the help of 23andMe data, they recently identified 57 genetic regions linked to stuttering in the human genome. Their findings represent a new breakthrough in how researchers think about speech conditions, genetics and the conditions that are linked to them. They're what some are calling a "quantum leap" in the field.Interested in more human biology and genetics episodes? Email us your question at [email protected] to every episode of Short Wave sponsor-free and support our work at NPR by signing up for Short Wave+ at plus.npr.org/shortwave.Learn more about sponsor message choices: podcastchoices.com/adchoicesNPR Privacy Policy
No persons identified in this episode.
No transcription available yet
Help us prioritize this episode for transcription by upvoting it.
Popular episodes get transcribed faster