23 September 2009 13:00
Autosomal recessive myotonic disease, distinct from channelopathy or dystrophy
Autosomal recessive myotonic disease, distinct from channelopathy or dystrophy
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
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
Autosomal dominant myotonic disease, distinct from channelopathy or dystrophy
Autosomal dominant myotonic disease, distinct from channelopathy or dystrophy
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(5 marks)