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
Developing a new gene therapy for periodic paralysis
Developing a mouse model and treatment for SORD neuropathy
Understanding the link between the shape of nuclei and DNA organisation in muscle cells from people living with laminopathy
Nerve or Muscle? Examining the cause of Charcot-Marie-Tooth disease
By ellen moye
Diagnosis of primary mitochondrial myopathies using MRI to measure how muscles use oxygen
By ellen moye