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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Ann Clin Transl Neurol
Main Authors: de Calbiac, Hortense, Dabacan, Adriana, Marsan, Elise, Tostivint, Hervé, Devienne, Gabrielle, Ishida, Saeko, Leguern, Eric, Baulac, Stéphanie, Muresan, Raul C., Kabashi, Edor, Ciura, Sorana
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2018
Teme:
Research Articles
Online dostop: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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