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Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A
- Correspondence to: Dr F Brancati, CSS Mendel Institute, Viale Regina Margherita, 261, 00198 Rome, Italy; f.brancati{at}css-mendel.it
Citation
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A
Publication history
- Received December 13, 2002
- Revised March 4, 2003
- First published August 21, 2003.
Online issue publication
April 13, 2016
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Copyright 2003 Journal of Neurology Neurosurgery and Psychiatry