Condition: MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL
rs121909502
in
CHRND
gene and
MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL
PMID 8872460
1996 New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.
PMID 11782989
2002 Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms.