Congenital myasthenic syndrome 8

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the AGRN gene.

Also known as: AGRN congenital myasthenic syndrome, CMS8, congenital myasthenic syndrome 8, congenital myasthenic syndrome caused by mutation in AGRN, congenital myasthenic syndrome type 8, myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects, myasthenic syndrome, congenital, type 8, myasthenic syndrome, congenital, 8

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