Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization

Wang, HCSalter, CGRefai, OHardy, HBarwick, KESAkpulat, UKvarnung, MChioza, BAHarlalka, GTaylan, FSejersen, TWright, JZimmerman, HHKarakaya, MStuve, BWeis, JSchara, URussell, MAAbdul-Rahman, OAChilton, JBlakely, RDBaple, ELCirak, SCrosby, AH2023-04-182023-04-182017.01.010006-8950https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=dspace_ku&SrcAuth=WosAPI&KeyUT=WOS:000414357800016&DestLinkType=FullRecord&DestApp=WOShttps://hdl.handle.net/20.500.12597/9726Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localizationArticle10.1093/brain/awx249WOS:000414357800016283828501401460-2156