Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency
We studied two families with five affected members suffering from ptosis and slowly progressive limb-girdle muscle weakness. All patients had abnormal decremental response on low-frequency nerve stimulation, but there were no repetitive responses to single stimuli. The patients improved on anti-acet...
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Veröffentlicht in: | Neurology 1998, Vol.50 (1), p.54-61 |
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