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Myotonia Congenita Mutation Enhances the Degradation of Human CLC-1 Chloride Channels
Myotonia congenita is a hereditary muscle disorder caused by mutations in the human voltage-gated chloride (Cl(−)) channel CLC-1. Myotonia congenita can be inherited in an autosomal recessive (Becker type) or dominant (Thomsen type) fashion. One hypothesis for myotonia congenita is that the inherita...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3570542/ https://ncbi.nlm.nih.gov/pubmed/23424641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0055930 |
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