Whole-exome sequencing of patients with juvenile myoclonic epilepsy

Background. Juvenile myoclonic epilepsy (JME) is the most common type of idiopathic generalized epilepsy with onset in adolescence and adulthood. During medical genetic counseling in probands with JME, aggravated epilepsy-related heredity is often detected. However, specific genetic variants of JME...

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מידע ביבליוגרפי

Principais autores:	E. E. Timechko, O. S. Shilkina, N. V. Oreshkova, V. O. Kobanenko, E. A. Osipova, N. A. Shnayder, D. V. Dmitrenko
פורמט:	Artigo
שפה:	Russo
יצא לאור:	IRBIS LLC 2022-10-01
סדרה:	Эпилепсия и пароксизмальные состояния
נושאים:	juvenile myoclonic epilepsy genetic generalized epilepsy gene whole exome sequencing pathogenic variant
גישה מקוונת:	https://www.epilepsia.su/jour/article/view/821
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!