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De Novo Coding Variants Are Strongly Associated With Tourette Disorder

De Novo Coding Variants Are Strongly Associated With Tourette Disorder. New research led by UC San Francisco scientists Jeremy Willsey and Matthew State has identified four likely risk genes with multiple de novo variants connected with Tourette disorder. This discovery promises to further our understanding of the genetic factors contributing to Tourette disorder and point to further gene discoveries using exome studies.



Article DOI: 10.1016/j.neuron.2017.04.024
Contributed by: David Simmons



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