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A CACNA1A variant associated with trigeminal neuralgia alters the gating of Cav2.1 channels
A novel missense mutation in the CACNA1A gene that encodes the pore forming α(1) subunit of the Ca(V)2.1 voltage-gated calcium channel was identified in a patient with trigeminal neuralgia. This mutation leads to a substitution of proline 2455 by histidine (P2455H) in the distal C-terminus region of...
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| Publicado no: | Mol Brain |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7789175/ https://ncbi.nlm.nih.gov/pubmed/33413531 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-020-00725-y |
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