Title : Novel COLQ mutation 950delC in synaptic congenital myasthenic syndrome and symptomatic heterozygous relatives - Schreiner_2007_Neuromuscul.Disord_17_262 |
Author(s) : Schreiner F , Hoppenz M , Klaeren R , Reimann J , Woelfle J |
Ref : Neuromuscular Disorders , 17 :262 , 2007 |
Abstract : Schreiner_2007_Neuromuscul.Disord_17_262 |
ESTHER : Schreiner_2007_Neuromuscul.Disord_17_262 |
PubMedSearch : Schreiner_2007_Neuromuscul.Disord_17_262 |
PubMedID: 17300939 |
Schreiner F, Hoppenz M, Klaeren R, Reimann J, Woelfle J (2007)
Novel COLQ mutation 950delC in synaptic congenital myasthenic syndrome and symptomatic heterozygous relatives
Neuromuscular Disorders
17 :262
Schreiner F, Hoppenz M, Klaeren R, Reimann J, Woelfle J (2007)
Neuromuscular Disorders
17 :262