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Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review
Objective: To verify the diagnosis of channelopathies in two families and explore the mechanism of the overlap between periodic paralysis (PP) and paramyotonia congenita (PMC). Methods: We have studied two cases with overlapping symptoms of episodic weakness and stiffness in our clinical center usin...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Taylor & Francis
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527082/ https://www.ncbi.nlm.nih.gov/pubmed/30931713 http://dx.doi.org/10.1080/19336950.2019.1600967 |