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An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis
Cannon reviews new evidence supporting a key role for anomalous inward currents in the etiology of hypokalemic periodic paralysis.
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Rockefeller University Press
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715912/ https://www.ncbi.nlm.nih.gov/pubmed/29138267 http://dx.doi.org/10.1085/jgp.201711923 |
| _version_ | 1783283838659592192 |
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| author | Cannon, Stephen C. |
| author_facet | Cannon, Stephen C. |
| author_sort | Cannon, Stephen C. |
| collection | PubMed |
| description | Cannon reviews new evidence supporting a key role for anomalous inward currents in the etiology of hypokalemic periodic paralysis. |
| format | Online Article Text |
| id | pubmed-5715912 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | The Rockefeller University Press |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-57159122018-06-04 An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis Cannon, Stephen C. J Gen Physiol Commentary Cannon reviews new evidence supporting a key role for anomalous inward currents in the etiology of hypokalemic periodic paralysis. The Rockefeller University Press 2017-12-04 /pmc/articles/PMC5715912/ /pubmed/29138267 http://dx.doi.org/10.1085/jgp.201711923 Text en © 2017 Cannon http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
| spellingShingle | Commentary Cannon, Stephen C. An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
| title | An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
| title_full | An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
| title_fullStr | An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
| title_full_unstemmed | An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
| title_short | An atypical Ca(V)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
| title_sort | atypical ca(v)1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
| topic | Commentary |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715912/ https://www.ncbi.nlm.nih.gov/pubmed/29138267 http://dx.doi.org/10.1085/jgp.201711923 |
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