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Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293I
1. Missense mutations in the α-subunit of the human skeletal muscle sodium channel (hSkM1) have been detected in some heritable forms of myotonia. By recording Na(+) currents from cells transfected with cDNA encoding either wild-type or mutant hSkM1, we characterized the functional consequences of t...
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| Главные авторы: | , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Blackwell Science Inc
1998
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2231077/ https://ncbi.nlm.nih.gov/pubmed/9660885 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-7793.1998.685bj.x |
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