| Title : A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome - Abicht_2002_Brain_125_1005 |
| Author(s) : Abicht A , Stucka R , Schmidt C , Briguet A , Hopfner S , Song IH , Pongratz D , Muller-Felber W , Ruegg MA , Lochmuller H |
| Ref : Brain , 125 :1005 , 2002 |
| Abstract : Abicht_2002_Brain_125_1005 |
| ESTHER : Abicht_2002_Brain_125_1005 |
| PubMedSearch : Abicht_2002_Brain_125_1005 |
| PubMedID: 11960891 |
Abicht A, Stucka R, Schmidt C, Briguet A, Hopfner S, Song IH, Pongratz D, Muller-Felber W, Ruegg MA, Lochmuller H (2002)
A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome
Brain
125 :1005
Abicht A, Stucka R, Schmidt C, Briguet A, Hopfner S, Song IH, Pongratz D, Muller-Felber W, Ruegg MA, Lochmuller H (2002)
Brain
125 :1005