Help us better understand the causes of stuttering by joining our genetics study today!
The Murdoch Children’s Research Institute is appealing for volunteers aged 7+ with experience of stuttering (past or present) to participate in the NHMRC Centre of Research Excellence in Speech and Language’s ‘Genetics of Stuttering Study’.
New research from the study team: We found a new gene that causes a neurodevelopmental disorder, with speech impairment.Aug 7, 2019
About the 'Genetics of Stuttering Study’
The 'Genetics of Stuttering Study’ aims to pinpoint the genes that predispose individuals to stuttering, which could revolutionise future research into the causes, treatment and prevention of the disorder.
Stuttering or stammering is considered a disability that affects verbal communication – particularly the rhythm or flow of communication.
Although the exact cause of stuttering is yet to be determined, genetics does play a role in stuttering, and a number of genetic variants having been identified to date.
The study involves 15 investigators at eight sites in Australia, the UK, the USA and The Netherlands.
Study researchers are working to recruit 3,000 volunteers aged 7+ with a history of stuttering (past or present) into the study. For now, only individuals within Australia can take part. We will be starting to recruit from other countries very soon - watch this space!
Participating in this study could make a genuine contribution to solving this disorder.
How can you help?
If you currently live with, or have a history of stuttering, we encourage you to volunteer for our groundbreaking research study by completing the 10 minute core component of our online survey. Depending on your responses to our survey, you may be asked to donate a saliva sample.
To help us meet our target of 3,000 participants by December 31, 2019, volunteer for our study today