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Read some of our latest blog posts below and stay up to date on the life-saving breakthroughs that you’re supporting.

Artwork for Perkins Reflect RAP – Expression of Interest

Harry Perkins Institute of Medical Research The Perkins conducts innovative research into the diseases that most affect families in the WA community and the world at large. We have grown…

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Genetic Variants Linked to Severe Form of Muscular Dystrophy

Researchers from Perth’s Harry Perkins Institute of Medical Research have led a study that uncovered changes in a gene associated with a rare and severe form of muscular dystrophy. The…

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Gene Mutation Discovery Sheds Light on Rare Muscle Disorder

A groundbreaking study led by Dr Mridul Johari and Associate Professor Gina Ravenscroft, has identified that a genetic mutation is responsible for a rare and debilitating form of congenital myopathy.…

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