| Title : Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutation - Sieb_2000_Ann.Neurol_48_379 |
| Author(s) : Sieb JP , Kraner S , Schrank B , Reitter B , Goebel TH , Tzartos SJ , Steinlein OK |
| Ref : Annals of Neurology , 48 :379 , 2000 |
| Abstract : Sieb_2000_Ann.Neurol_48_379 |
| ESTHER : Sieb_2000_Ann.Neurol_48_379 |
| PubMedSearch : Sieb_2000_Ann.Neurol_48_379 |
| PubMedID: 10976646 |
Sieb JP, Kraner S, Schrank B, Reitter B, Goebel TH, Tzartos SJ, Steinlein OK (2000)
Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutation
Annals of Neurology
48 :379
Sieb JP, Kraner S, Schrank B, Reitter B, Goebel TH, Tzartos SJ, Steinlein OK (2000)
Annals of Neurology
48 :379