Abdul-Rahman OA

References (2)

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

Title : Neuromotor synapses in Escobar syndrome - Robinson_2013_Am.J.Med.Genet.A_161_3042
Author(s) : Robinson KG , Viereck MJ , Margiotta MV , Gripp KW , Abdul-Rahman OA , Akins RE
Ref : American Journal of Medicine Genet A , 161 :3042 , 2013
Abstract : Robinson_2013_Am.J.Med.Genet.A_161_3042
ESTHER : Robinson_2013_Am.J.Med.Genet.A_161_3042
PubMedSearch : Robinson_2013_Am.J.Med.Genet.A_161_3042
PubMedID: 24038971