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 https://medicine.vumc.org/department-directory/Jennifer-Below and Dillon Pruett https://fda.fsu.edu/nfd/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] mailto:[email protected]. Listen 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 http://plus.npr.org/shortwave. See pcm.adswizz.com https://pcm.adswizz.com for information about our collection and use of personal data for sponsorship and to manage your podcast sponsorship preferences. NPR Privacy Policy https://www.npr.org/about-npr/179878450/privacy-policy
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