Congenital myasthenic syndrome 19

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the COL13A1 gene.

Also known as: CMS19, COL13A1 congenital myasthenic syndrome, congenital myasthenic syndrome caused by mutation in COL13A1, congenital myasthenic syndrome type 19, myasthenic syndrome, congenital, 19, myasthenic syndrome, congenital, type 19

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