Impaired cortico-striatal excitatory transmission triggers epilepsy-Reference-Cited by-同舟云学术

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Impaired cortico-striatal excitatory transmission triggers epilepsy

Published:2019-04-23 Issue:1 Volume:10 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Miyamoto Hiroyuki,Tatsukawa Tetsuya,Shimohata Atsushi,Yamagata Tetsushi,Suzuki Toshimitsu,Amano Kenji,Mazaki Emi,Raveau Matthieu,Ogiwara Ikuo,Oba-Asaka Atsuko,Hensch Takao K.,Itohara Shigeyoshi,Sakimura Kenji,Kobayashi Kenta,Kobayashi Kazuto,Yamakawa Kazuhiro

Funder

Japan Agency for Medical Research and Development

MEXT | JST | Precursory Research for Embryonic Science and Technology

Kawano Masanori Memorial Public Interest Incorporated Foundation

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/s41467-019-09954-9.pdf

Reference66 articles.

1. Kamiya, K. et al. A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline. J. Neurosci. 24, 2690–2698 (2004).

2. Saitsu, H. et al. De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy. Nat. Genet. 40, 782–788 (2008).

3. Ogiwara, I. et al. De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies. Neurology 73, 1046–1053 (2009).

4. Rauch, A. et al. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet 380, 1674–1682 (2012).

5. Hoischen, A., Krumm, N. & Eichler, E. E. Prioritization of neurodevelopmental disease genes by discovery of new mutations. Nat. Neurosci. 17, 764–772 (2014).

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