A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report
T Chang, J Cossins, D Beeson BMC Neurology 16: e195 2016https://doi.org/10.1186/s12883-016-0716-y
T Chang, J Cossins, D Beeson BMC Neurology 16: e195 2016https://doi.org/10.1186/s12883-016-0716-y
© 2024 Association of Sri Lankan Neurologists. All rights reserved. | Designed and Developed by Pentacove
