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Bibliografía
[1]
V. Dubowitz.
Metabolic Myopathies III Ion Channel Disorders.
Muscle disorders in childhood, pp. 266-314
[2]
J. Zhang, A.L. George Jr., R.C. Griggs, G.T. Fouad, J. Roberts, H. Kwiecinski, et al.
Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita.
Neurology, 47 (1996), pp. 993-998
[3]
C. De Diego, J. Gámez, E. Plassart-Schiess, A. Lasa, E. Del Río, C. Cervera, et al.
Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish families.
J Neurol, 246 (1999), pp. 825-829
[4]
J. Esteban, A.M. Neumeyer, D. McKenna-Yasek, R.H. Brown.
Identification of two mutations and a polymorphism in the chloride channel CLCN1 in patients with Becker’s generalized myotonia.
Neurogenetics, 1 (1998), pp. 185-188
[5]
K. Jurkat-Rott, H. Lerche, F. Lehmann-Horn.
Skeletal muscle channelopathies.
J Neurol, 249 (2002), pp. 1493-1502
[6]
H.C. Azevedo, L.I. Mendonca, P.N. Salum, M.S. Carvalho, S.K. Nagahashi- Marie, A.A. Siquiera-Carvalho, et al.
Gongenital myotonia. Report of 7 patients.
Arq Neuropsiquiatr, 54 (1996), pp. 595-600
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