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Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker
Missense mutations in the skeletal muscle Na+ channel alpha subunit occur in several heritable forms of myotonia and periodic paralysis. Distinct phenotypes arise from mutations at two sites within the III-IV cytoplasmic loop: myotonia without weakness due to substitutions at glycine 1306, and myoto...
Gorde:
| Formatua: | Artigo |
|---|---|
| Hizkuntza: | Inglês |
| Argitaratua: |
The Rockefeller University Press
1996
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2217015/ https://ncbi.nlm.nih.gov/pubmed/8740371 |
| Etiketak: |
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