Schreiner_2007_Neuromuscul.Disord_17_262

Reference

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

Related information

Citations formats

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