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New Project Funding to investigate congenital forms of muscular dystrophy

Project funding received from the Newlife Charity to investigate molecular and therapeutic mechanisms of a novel form of congenital muscular dystrophy

We're excited to be continuing our work on congenital muscular dystrophy thanks to a grant from the Newlife Foundation for Disabled Children. The project will follow up recent genetic findings in families with congenital muscular dystrophy resulting from mutations in novel genes. We hope to carry out preliminary experiments to understand the biological processes involved with the hope that these may provide future therapeutic targets.

 

 

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