| Title : Clinical and Molecular Analysis of a Novel COLQ Missense Mutation Causing Congenital Myasthenic Syndrome in a Syrian Family - Matlik_2014_Pediatr.Neurol_51_165 |
| Author(s) : Matlik HN , Milhem RM , Saadeldin IY , Al-Jaibeji HS , Al-Gazali L , Ali BR |
| Ref : Pediatr Neurol , 51 :165 , 2014 |
| Abstract : Matlik_2014_Pediatr.Neurol_51_165 |
| ESTHER : Matlik_2014_Pediatr.Neurol_51_165 |
| PubMedSearch : Matlik_2014_Pediatr.Neurol_51_165 |
| PubMedID: 24938146 |
Matlik HN, Milhem RM, Saadeldin IY, Al-Jaibeji HS, Al-Gazali L, Ali BR (2014)
Clinical and Molecular Analysis of a Novel COLQ Missense Mutation Causing Congenital Myasthenic Syndrome in a Syrian Family
Pediatr Neurol
51 :165
Matlik HN, Milhem RM, Saadeldin IY, Al-Jaibeji HS, Al-Gazali L, Ali BR (2014)
Pediatr Neurol
51 :165