Congenital myasthenic syndrome 20

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SLC5A7 gene.

Also known as: CMS20, SLC5A7 congenital myasthenic syndrome, congenital myasthenic syndrome caused by mutation in SLC5A7, congenital myasthenic syndrome type 20, myasthenic syndrome, congenital, 20, presynaptic

1 clinical trial for this condition and its sub-types.