Polyglucosan body myopathy type 2

Any polyglucosan body myopathy in which the cause of the disease is a mutation in the GYG1 gene.

Also known as: GYG1 polyglucosan body myopathy, polyglucosan body myopathy caused by mutation in GYG1, polyglucosan body myopathy type 2, PGBM2, polyglucosan body myopathy 2

60 clinical trials for this condition and its sub-types.