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Refai O

References (2)

Title : Dopamine-dependent, swimming-induced paralysis arises as a consequence of loss of function mutations in the RUNX transcription factor RNT-1 - Robinson_2019_PLoS.One_14_e0216417
Author(s) : Robinson SB , Refai O , Hardaway JA , Sturgeon S , Popay T , Bermingham DP , Freeman P , Wright J , Blakely RD
Ref : PLoS ONE , 14 :e0216417 , 2019
Abstract : Robinson_2019_PLoS.One_14_e0216417
ESTHER : Robinson_2019_PLoS.One_14_e0216417
PubMedSearch : Robinson_2019_PLoS.One_14_e0216417
PubMedID: 31083672

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