Myasthenic syndrome, congenital, 1B, fast-channel

MONDO:0012156

A congenital myasthenic syndrome characterized by defects in postsynaptic neuromuscular junctions with early-onset progressive muscle weakness that has material basis in mutation in the CHRNA1 gene on chromosome 2q.

Also known as: CMS1B, congenital myasthenic syndrome type 1B, myasthenic syndrome, congenital, 1B, fast-channel, congenital myasthenic syndrome 1B, myasthenic syndrome, congenital, 1B, FAST-channel

0 clinical trials for this condition and its sub-types, 0 tagged with Myasthenic syndrome, congenital, 1B, fast-channel itself.

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↑ Congenital myasthenic syndrome 1A (0)

Including sub-types (0) Tagged with Myasthenic syndrome, congenital, 1B, fast-channel (0)

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