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27. Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptor. Engel AG; Nagel A; Walls TJ; Harper CM; Waisburg HA Muscle Nerve; 1993 Dec; 16(12):1284-92. PubMed ID: 8232383 [TBL] [Abstract][Full Text] [Related]
28. Desensitization of mutant acetylcholine receptors in transgenic mice reduces the amplitude of neuromuscular synaptic currents. Bhattacharyya BJ; Day JW; Gundeck JE; Leonard S; Wollmann RL; Gomez CM Synapse; 1997 Dec; 27(4):367-77. PubMed ID: 9372559 [TBL] [Abstract][Full Text] [Related]
29. Clinical neurophysiology of disorders of the neuromuscular junction. Sanders DB J Clin Neurophysiol; 1993 Apr; 10(2):167-80. PubMed ID: 8389381 [TBL] [Abstract][Full Text] [Related]
30. [Diagnostic aspects of myasthenia gravis]. Friedli WG Schweiz Rundsch Med Prax; 1989 Sep; 78(38):1037-44. PubMed ID: 2552554 [TBL] [Abstract][Full Text] [Related]
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34. Mutation of the acetylcholine receptor epsilon-subunit promoter in congenital myasthenic syndrome. Nichols P; Croxen R; Vincent A; Rutter R; Hutchinson M; Newsom-Davis J; Beeson D Ann Neurol; 1999 Apr; 45(4):439-43. PubMed ID: 10211467 [TBL] [Abstract][Full Text] [Related]
36. A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions. Chevessier F; Girard E; Molgó J; Bartling S; Koenig J; Hantaï D; Witzemann V Hum Mol Genet; 2008 Nov; 17(22):3577-95. PubMed ID: 18718936 [TBL] [Abstract][Full Text] [Related]
37. Neurophysiological aspects of diagnosis in neuromuscular transmission defects--an update. Stålberg E Electroencephalogr Clin Neurophysiol Suppl; 1999; 50():377-85. PubMed ID: 10689484 [No Abstract] [Full Text] [Related]
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