A new explanation for recessive myotonia congenital: Exon deletions and duplications in CLCN1

D. L. Raja Rayan, A. Haworth, R. Sud, E. Matthews, D. Fialho, J. Burge, S. Portaro, S. Schorge, K. Tuin, P. Lunt, M. McEntagart, A. Toscano, M. B. Davis, M. G. Hanna

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