Refai O

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 :

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 :

PubMedSearch : Wang_2017_Brain_140_2838

PubMedID: 29088354

Refai O

References (2)

1. 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

2. Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization - Wang_2017_Brain_140_2838