GENETIC MARKERS OF CATAMENIAL EPILEPSY IN WOMEN

Please use this identifier to cite or link to this item: http://repository.tma.uz/xmlui/handle/1/5530

Title:	GENETIC MARKERS OF CATAMENIAL EPILEPSY IN WOMEN
Authors:	Muratov F.Kh., Yusupova D.Y
Issue Date:	2022
Publisher:	ФУНДАМЕНТАЛ ВА КЛИНИК ТИББИЁТ АХБОРОТНОМАСИ
Abstract:	Objective: to study the role of the sodium channel gene (SCN1A) in the development of catamenialepilepsy. Materials and research methods: molecular genetic studies with determination of the frequency of alleles of the SCN1A gene were performed in 100 women examined by us. Of these, 60 patients with catamenial epilepsy, 20 with symptomatic epilepsy.
URI:	http://repository.tma.uz/xmlui/handle/1/5530
Appears in Collections:	Thesis, Articles

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Муратов Ф.Х., Юсупова Д.Ю махаллий тезис 2.pdf	GENETIC MARKERS OF CATAMENIAL EPILEPSY IN WOMEN	735.14 kB	Adobe PDF	View/Open

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