Identifying biomarkers for congenital and limb girdle muscular dystrophies

  • Identifying biomarkers for congenital and limb girdle muscular dystrophies

    Professor Muntoni and his team are searching for biomarkers for monitoring the progression of congenital and limb girdle muscular dystrophies.

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  • Prof Darren Monckton

    Understanding the genetics of myotonic dystrophy type 1

    Professor Monckton and his team are investigating links between genetic changes and the symptoms of myotonic dystrophy type 1.

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  • Peter Zammit

    Generating a model of FSHD and testing a potential therapeutic approach

    Professor Zammit and his team at King’s College London are generating a mouse model that will allow a greater understanding of the genetics underlying facioscapulohumeral muscular dystrophy.

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  • Professor Wood in his lab, University of Oxford

    Developing a genetic therapy for spinal muscular atrophy

    Professor Matthew Wood and his team are developing ways of improving the delivery of a potential genetic therapy for spinal muscular atrophy.

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  • Understanding cell membrane changes in centronuclear myopathy and Charcot-Marie-Tooth disease

    Dr Andrew Shevchuk is studying cell membrane changes and how these functions are altered in centronuclear myopathy and Charcot-Marie-Tooth disease.

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