Hippocampus-related cognitive disorders develop in the absence of epilepsy and ataxia in the heterozygous <i>Cacna1a</i> mutant mice <i>tottering</i>-Reference-Cited by-同舟云学术

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Hippocampus-related cognitive disorders develop in the absence of epilepsy and ataxia in the heterozygous Cacna1a mutant mice tottering

Published:2022-05-12 Issue:1 Volume:16 Page:113-126
ISSN:1933-6950
Container-title:Channels
language:en
Short-container-title:Channels

Author:

Nakao Akito¹^ORCID,Hayashida Katsumi¹,Ogura Hiroo²,Mori Yasuo¹,Imoto Keiji³^ORCID

Affiliation:

1. Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan

2. Product Creation Headquarters, Eisai Corporate, Limited, Tokyo, Japan

3. Division of Neural Signaling, Department of Information Physiology, National Institute for Physiological Sciences, Okazaki, Japan

Funder

JSPS KAKENHI

Publisher

Informa UK Limited

Subject

Biochemistry,Biophysics

Link

https://www.tandfonline.com/doi/pdf/10.1080/19336950.2022.2072449

Reference56 articles.

1. Primary structure and functional expression from complementary DNA of a brain calcium channel

2. Calcium Channels, Synaptic Plasticity, and Neuropsychiatric Disease

3. Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia

4. Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

5. Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The genotype–phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews;Frontiers in Molecular Neuroscience;2023-07-24

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