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. 2003 Sep;74(9):1339–1341. doi: 10.1136/jnnp.74.9.1339
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A
F Brancati
1, E Valente
1, N Davies
1, A Sarkozy
1, M Sweeney
1, M LoMonaco
1, A Pizzuti
1, M Hanna
1, B Dallapiccola
1
F Brancati
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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E Valente
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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N Davies
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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A Sarkozy
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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M Sweeney
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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M LoMonaco
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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A Pizzuti
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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M Hanna
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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B Dallapiccola
1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
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1Department of Experimental Medicine and Pathology, "La Sapienza" University, Rome, Italy. f.brancati@css-mendel.it
PMCID: PMC1738672 PMID: 12933953