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Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A.
F Brancati, E M Valente, N P Davies, A Sarkozy, M G Sweeney, M LoMonaco, A Pizzuti, M G Hanna, B Dallapiccola
J Neurol Neurosurg Psychiatry 2003; 74(9):1339-1341
ICID: 683441
IC™ Value: 13.02
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