Wang_2017_Brain_140_2838

Reference

Title : Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization - Wang_2017_Brain_140_2838
Author(s) : Wang H , Salter CG , Refai O , Hardy H , Barwick KES , Akpulat U , Kvarnung M , Chioza BA , Harlalka G , Taylan F , Sejersen T , Wright J , Zimmerman HH , Karakaya M , Stuve B , Weis J , Schara U , Russell MA , Abdul-Rahman OA , Chilton J , Blakely RD , Baple EL , Cirak S , Crosby AH
Ref : Brain , 140 :2838 , 2017
Abstract : Wang_2017_Brain_140_2838
ESTHER : Wang_2017_Brain_140_2838
PubMedSearch : Wang_2017_Brain_140_2838
PubMedID: 29088354

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Citations formats

Wang H, Salter CG, Refai O, Hardy H, Barwick KES, Akpulat U, Kvarnung M, Chioza BA, Harlalka G, Taylan F, Sejersen T, Wright J, Zimmerman HH, Karakaya M, Stuve B, Weis J, Schara U, Russell MA, Abdul-Rahman OA, Chilton J, Blakely RD, Baple EL, Cirak S, Crosby AH (2017)
Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization
Brain 140 :2838

Wang H, Salter CG, Refai O, Hardy H, Barwick KES, Akpulat U, Kvarnung M, Chioza BA, Harlalka G, Taylan F, Sejersen T, Wright J, Zimmerman HH, Karakaya M, Stuve B, Weis J, Schara U, Russell MA, Abdul-Rahman OA, Chilton J, Blakely RD, Baple EL, Cirak S, Crosby AH (2017)
Brain 140 :2838