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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Vydáno v:Ann Clin Transl Neurol
Hlavní autoři: de Calbiac, Hortense, Dabacan, Adriana, Marsan, Elise, Tostivint, Hervé, Devienne, Gabrielle, Ishida, Saeko, Leguern, Eric, Baulac, Stéphanie, Muresan, Raul C., Kabashi, Edor, Ciura, Sorana
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2018
Témata:
Research Articles
On-line přístup: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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