23 September 2009 13:00
Autoimmune neurological channelopathy due to a p/q-type voltage gated calcium channel defect
Autoimmune neurological channelopathy due to a p/q-type voltage gated calcium channel defect
Autosomal dominant myotonic disease, distinct from channelopathy or dystrophy
Autosomal dominant myotonic disease, distinct from channelopathy or dystrophy
Autoimmune neurological channelopathy due to a acetylcholine receptor subunits defect
Autoimmune neurological channelopathy due to a acetylcholine receptor subunits defect
Autoimmune neurological channelopathy due to a potassium channel defect
Autoimmune neurological channelopathy due to a potassium channel defect
1
(4 marks)