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Depdc5 knockdown causes mTOR‐dependent motor hyperactivity in zebrafish
OBJECTIVE: DEPDC5 was identified as a major genetic cause of focal epilepsy with deleterious mutations found in a wide range of inherited forms of focal epilepsy, associated with malformation of cortical development in certain cases. Identification of frameshift, truncation, and deletion mutations i...
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| Publicado no: | Ann Clin Transl Neurol |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5945968/ https://ncbi.nlm.nih.gov/pubmed/29761115 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.542 |
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