Search Results - Akpulat, U.

  • Showing 1 - 2 results of 2
Refine Results
  1. 1
    Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization

    Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization by Wang, Haicui, Salter, Claire G, Refai, Osama, Hardy, Holly, Barwick, Katy E S, Akpulat, Ugur, Kvarnung, Malin, Chioza, Barry A, Harlalka, Gaurav, Taylan, Fulya, Sejersen, Thomas, Wright, Jane, Zimmerman, Holly H, Karakaya, Mert, Stüve, Burkhardt, Weis, Joachim, Schara, Ulrike, Russell, Mark A, Abdul-Rahman, Omar A, Chilton, John, Blakely, Randy D, Baple, Emma L, Cirak, Sebahattin, Crosby, Andrew H

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    P.6.a.005 The role of dopamine 2 receptor gene and personality characteristics in alcohol dependence in Turkish population

    P.6.a.005 The role of dopamine 2 receptor gene and personality characteristics in alcohol dependence in Turkish population by Kitis, A., Akvardar, Y., Eresen, C., Kizildag, S., Akpulat, U., Yildirimcan, S., Alptekin, K., Akdede, B.B., Arkar, H.

    Get full text
    Article
    Save to List
    Saved in:

Search Tools: