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Monogenic Epilepsies: Disease Mechanisms, Clinical Phenotypes, and Targeted Therapies
A monogenic etiology can be identified in up to 40% of people with severe epilepsy. To address earlier and more appropriate treatment strategies, clinicians are required to know the implications that specific genetic causes might have on pathophysiology, natural history, comorbidities, and treatment...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336826/ https://www.ncbi.nlm.nih.gov/pubmed/34493617 http://dx.doi.org/10.1212/WNL.0000000000012744 |