Professor David Thorburn

Group Leader, Brain & Mitochondrial Research, Murdoch Children's Research Institute (MCRI); Honorary Professorial Fellow, Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne

Health & Medicine

Research

Cutting the diagnosis journey for children born with rare genetic diseases

Families can wait years for a diagnosis of a rare genetic disorder, but a new test can provide answers in days for a better understanding of the condition and potentially earlier treatment