Genes at the junction—candidates for congenital myasthenic syndromes

• 1 January 1997
• journal article
• review article
• Published by Elsevier in Trends in Neurosciences
• Vol. 20  (1) , 15-22
• https://doi.org/10.1016/s0166-2236(96)10066-7

Abstract

Keywords

• ACETYLCHOLINE RECEPTOR
• ACETYLCHOLINESTERASE
• CONGENITAL MYASTHENIC SYNDROME
• NEUROMUSCULAR JUNCTION
• SLOW CHANNEL SYNDROME
• CENTRAL NERVOUS SYSTEM
• POINT MUTATION
• GENETICS
• AMINO ACID
• ION CHANNEL