טוען...
Familial hemiplegic migraine mutations increase Ca(2+) influx through single human Ca(V)2.1 channels and decrease maximal Ca(V)2.1 current density in neurons
Insights into the pathogenesis of migraine with aura may be gained from a study of human Ca(V)2.1 channels containing mutations linked to familial hemiplegic migraine (FHM). Here, we extend the previous single-channel analysis to human Ca(V)2.1 channels containing mutation V1457L. This mutation incr...
שמור ב:
| Main Authors: | , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
The National Academy of Sciences
2002
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC130625/ https://ncbi.nlm.nih.gov/pubmed/12235360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.192242399 |
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