Congenital myasthenic syndrome 1A

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the CHRNA1 gene.

Also known as: CHRNA1 congenital myasthenic syndrome, CMS1A, congenital myasthenic syndrome caused by mutation in CHRNA1, congenital myasthenic syndrome type 1A, Cms IIa, Cms IIa, formerly, myasthenic syndrome, congenital, 1A, slow-channel, myasthenic syndrome, congenital, type IIa

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