2019年11月
De novo NSF mutations cause early infantile epileptic encephalopathy.
Annals of clinical and translational neurology
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- 巻
- 6
- 号
- 11
- 開始ページ
- 2334
- 終了ページ
- 2339
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1002/acn3.50917
N-ethylmaleimide-sensitive factor (NSF) plays a critical role in intracellular vesicle transport, which is essential for neurotransmitter release. Herein, we, for the first time, document human monogenic disease phenotype of de novo pathogenic variants in NSF, that is, epileptic encephalopathy of early infantile onset. When expressed in the developing eye of Drosophila, the mutant NSF severely affected eye development, while the wild-type allele had no detectable effect under the same conditions. Our findings suggest that the two pathogenic variants exert a dominant negative effect. De novo heterozygous mutations in the NSF gene cause early infantile epileptic encephalopathy.
- リンク情報
- ID情報
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- DOI : 10.1002/acn3.50917
- PubMed ID : 31675180
- PubMed Central 記事ID : PMC6856629