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Second‐hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA
Focal cortical dysplasia (FCD) causes drug‐resistant epilepsy and is associated with pathogenic variants in mTOR pathway genes. How germline variants cause these focal lesions is unclear, however a germline + somatic “2‐hit” model is hypothesized. In a boy with drug‐resistant epilepsy, FCD, and a ge...
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| Publicado en: | Ann Clin Transl Neurol |
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| Main Authors: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6649645/ https://ncbi.nlm.nih.gov/pubmed/31353856 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50815 |
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