Browsing by Author "Harlalka, G"
Now showing 1 - 1 of 1
- Results Per Page
- Sort Options
Web of Science Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization(2017.01.01) Wang, HC; 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