Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita

J. Zhang, A. L. George, R. C. Griggs, G. T. Fouad, J. Roberts, H. Kwieciński, A. M. Connolly, L. J. Ptáček*

*Corresponding author for this work

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Medicine & Life Sciences