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Hypokalemic periodic paralysis due to CACNA1S gene mutation
Hypokalemic periodic paralysis (HypoPP) is a relatively rare but treatable disorder caused by mutations in the CACNA1S gene. HypoPP patients may experience paralytic episodes associated with hypokalemia and, infrequently, may develop late-onset proximal myopathy. The paralytic attacks are characteri...
Shranjeno v:
| izdano v: | Neurosciences (Riyadh) |
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| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Riyadh : Armed Forces Hospital
2019
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8015512/ https://ncbi.nlm.nih.gov/pubmed/31380823 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17712/nsj.2018.3.20180005 |
| Oznake: |
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