Developing a triple-action treatment for Duchenne muscular dystrophy
By vinnie
Exploring new tools to correct gene changes in muscle wasting conditions
By vinnie
Understanding how DUX4 causes muscle damage in facioscapulohumeral muscular dystrophy
By vinnie
Improving how scientists identify new potential treatments for FSHD
By vinnie
TRANSFORM-CMT: Preparing for clinical trials in Charcot-Marie-Tooth disease
Investigating if a gene change can protect muscles in merosin-deficient congenital muscular dystrophy
Developing next-generation therapies for LMNA-related congenital muscular dystrophy using ‘mini muscle’ models
Improving the delivery of treatments for collagen VI-related muscular dystrophy
Using brain imaging to study myotonic dystrophy
Understanding how Duchenne muscular dystrophy affects brain function
By amber sunner
Using state-of-the-art genetic sequencing techniques to find genes that cause limb-girdle muscular dystrophies
By ellen moye