Time‐limited alterations in cortical activity of a knock‐in mouse model of <i>KCNQ2</i> ‐related developmental and epileptic encephalopathy-Reference-Cited by-同舟云学术

Time‐limited alterations in cortical activity of a knock‐in mouse model of KCNQ2 ‐related developmental and epileptic encephalopathy

Published:2022-04-27 Issue:10 Volume:600 Page:2429-2460
ISSN:0022-3751
Container-title:The Journal of Physiology
language:en
Short-container-title:The Journal of Physiology

Author:

Biba‐Maazou Najoua¹,Becq Hélène¹,Pallesi‐Pocachard Emilie¹,Sarno Stefania¹,Granjeaud Samuel²^ORCID,Montheil Aurélie¹,Kurz Marie¹,Villard Laurent³⁴,Milh Mathieu³⁵,Santini Pierre‐Pascal Lenck¹,Aniksztejn Laurent¹^ORCID

Affiliation:

1. INSERM, INMED Aix‐Marseille University Turing Centre for Living Systems Marseille France

2. Centre de Recherche en Cancérologie de Marseille, INSERM, U1068, Institut Paoli Calmettes, CNRS, UMR7258 Aix‐Marseille University UM 105 Marseille France

3. Aix‐Marseille University INSERM, Marseille Medical Genetics Centre (MMG) Marseille France

4. Department of Medical Genetics La Timone Children's Hospital Marseille France

5. Department of Pediatric Neurology La Timone Children's Hospital Marseille France

Publisher

Wiley

Subject

Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1113/JP282536

Reference81 articles.

1. A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels

2. M-currents and other potassium currents in bullfrog sympathetic neurones

3. The variable phenotypes of KCNQ-related epilepsy

4. Genetic potassium channel-associated epilepsies: Clinical review of the Kv family

5. Sequential Generation of Two Distinct Synapse-Driven Network Patterns in Developing Neocortex

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