|  Title : Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea - Bauche_2016_Am.J.Hum.Genet_99_753 | 
    
    
        
        | Author(s) : 
                            Bauche S ,                             O'Regan S ,                             Azuma Y ,                             Laffargue F ,                             McMacken G ,                             Sternberg D ,                             Brochier G ,                             Buon C ,                             Bouzidi N ,                             Topf A ,                             Lacene E ,                             Remerand G ,                             Beaufrere AM ,                             Pebrel-Richard C ,                             Thevenon J ,                             El Chehadeh-Djebbar S ,                             Faivre L ,                             Duffourd Y ,                             Ricci F ,                             Mongini T ,                             Fiorillo C ,                             Astrea G ,                             Burloiu CM ,                             Butoianu N ,                             Sandu C ,                             Servais L ,                             Bonne G ,                             Nelson I ,                             Desguerre I ,                             Nougues MC ,                             Boeuf B ,                             Romero N ,                             Laporte J ,                             Boland A ,                             Lechner D ,                             Deleuze JF ,                             Fontaine B ,                             Strochlic L ,                             Lochmuller H ,                             Eymard B ,                             Mayer M ,                             Nicole S                      | 
    
    
    
        | 
            Ref : 
            American Journal of Human Genetics            , 99            :753            , 2016         | 
    
        
        | 
            Abstract :  
                            
                
                
                     | 
    
    
        | PubMedSearch : Bauche_2016_Am.J.Hum.Genet_99_753 | 
    
    
    
        | PubMedID: 27569547 |