Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations - RCFM (EN)

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Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations

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We are a center of excellence for neuromuscular diseases (NMD).

We believe in seing the entire person with NMD in a life-long perspective. That way, we can help create the best environment for people with NMD and their families.

We share our knowledge with our patients, their families and our professional partners. We work interdisciplinary and across sectors.

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Newly diagnosed?
Research
The EK scale

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