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
| Autor: | Plassart, E., Reboul, J., Recan, D., Millasseau, P., Eymard, B., Pelletier, J., Thomas, C., Chapon, F., Desnuelle, C., Confavreux, C., Bady, B., Martin, Jean-Jacques, Lenoir, G., Serratrice, G., Fardeau, M., Fontaine, Bertrand |
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| Jazyk: | angličtina |
| Rok vydání: | 1994 |
| Zdroj: | European journal of human genetics |
| ISSN: | 1018-4813 |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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