DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Plassart E, Reboul J, Rime CS , et al.
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations.
Eur J Hum Genet 1994;
2 (2) 110-124
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