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Gain‐of‐function mutation Met136Val in SCN8A may not be a common cause of trigeminal neuralgia
BACKGROUND: The Met136Val mutation in SCN8A was described in a case of trigeminal neuralgia but no frequency among affected individuals was provided. METHODS: Direct sequencing of 123 individuals diagnosed with classic trigeminal neuralgia was performed aimed to detect the Met136Val change. RESULTS:...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077135/ https://www.ncbi.nlm.nih.gov/pubmed/33428824 http://dx.doi.org/10.1002/mgg3.1587 |