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| 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 : Huze_2009_Am.J.Hum.Genet_85_155 |
| ESTHER : Huze_2009_Am.J.Hum.Genet_85_155 |
| PubMedSearch : Huze_2009_Am.J.Hum.Genet_85_155 |
| PubMedID: 19631309 |