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Mitochondrial DNA analyses found five novel mutations in idiopathic epilepsy patients
Epilepsy is a common and chronic neurological disease with a high degree of genetic heterogeneity. The etiology and pathogenesis of the disease have not been fully understood. Many studies suggested that there was a reciprocal relationship between mitochondrial dysfunction and epilepsy, but few stud...
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/PMC7707843/ https://www.ncbi.nlm.nih.gov/pubmed/33365557 http://dx.doi.org/10.1080/23802359.2019.1633963 |