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1 Possible Causes for Progressive Disorder due to Secondary Myopathy

  • Slow-Channel Congenital Myasthenic Syndrome

    Mutations in genes encoding the epsilon, delta, beta and alpha subunits of the end plate acetylcholine (ACh) receptor (AChR) are described and functionally characterized in three slow-channel congenital myasthenic syndrome patients. All three had prolonged end plate currents and AChR channel opening episodes and[…][]

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