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Brancaccio A

References (2)

Title : Identification of an agrin mutation that causes congenital myasthenia and affects synapse function - Huze_2009_Am.J.Hum.Genet_85_155
Author(s) : Huze C , Bauche S , Richard P , Chevessier F , Goillot E , Gaudon K , Ben Ammar A , Chaboud A , Grosjean I , Lecuyer HA , Bernard V , Rouche A , Alexandri N , Kuntzer T , Fardeau M , Fournier E , Brancaccio A , Ruegg MA , Koenig J , Eymard B , Schaeffer L , Hantai D
Ref : American Journal of Human Genetics , 85 :155 , 2009
Abstract :
PubMedSearch : Huze_2009_Am.J.Hum.Genet_85_155
PubMedID: 19631309

Title : Alternative splicing of agrin alters its binding to heparin, dystroglycan, and the putative agrin receptor - Gesemann_1996_Neuron_16_755
Author(s) : Gesemann M , Cavalli V , Denzer AJ , Brancaccio A , Schumacher B , Ruegg MA
Ref : Neuron , 16 :755 , 1996
Abstract :
PubMedSearch : Gesemann_1996_Neuron_16_755
PubMedID: 8607994