Severe <i>KCNT1</i>-related developmental and epileptic encephalopathy

Severe <i>KCNT1</i>-related developmental and epileptic encephalopathy

Developmental and epileptic encephalopathy (DEE) caused by a mutation in the KCNT1 gene (KCNT1-DEE) is registered in the Online Mendelian Inheritance in Man (OMIM) catalogue inder code number 614959. Alternative names: DEE 14, early infantile epileptic encephalopathy 14. KCNT1-DEE most often manifes...

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Bibliographic Details
Main Authors:	A. G. Malov, L. Yu. Brokhin, A. V. Veselkova
Format:	Article
Language:	Russian
Published:	IRBIS LLC 2025-07-01
Series:	Эпилепсия и пароксизмальные состояния
Subjects:	<i>kcnt1</i>-related developmental and epileptic encephalopathy developmental and epileptic encephalopathy 14 early infantile epileptic encephalopathy type 14
Online Access:	https://www.epilepsia.su/jour/article/view/1211
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