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A novel KCNT1 mutation in a Chinese family with severe auto..:
Xie Na
;
Qin Weiwei
;
Deng Jianzhong
...
https://doi.org/10.1515/tnsci-2020-0182. , 2021
Link:
https://doi.org/10.1515/tnsci-2020-0182
RT Journal T1
A novel KCNT1 mutation in a Chinese family with severe autosomal-dominant nocturnal frontal lobe epilepsy
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:212d8405c589450b98e83756c5795c27&Exemplar=1&LAN=DE A1 Xie Na A1 Qin Weiwei A1 Deng Jianzhong A1 Qi Jinxing A1 Niu Dewang A1 Lu Guifeng A1 Wang Qun PB De Gruyter YR 2021 K1 kcnt1 K1 severe adnfle K1 autosomal dominant K1 refractory epilepsy K1 psychiatric symptoms K1 Neurosciences. Biological psychiatry. Neuropsychiatry K1 RC321-571 JF https://doi.org/10.1515/tnsci-2020-0182 LK http://dx.doi.org/https://doi.org/10.1515/tnsci-2020-0182 DO https://doi.org/10.1515/tnsci-2020-0182 SF ELIB - SuUB Bremen
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