GENETIC MARKERS OF CATAMENIAL EPILEPSY IN WOMEN

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DC Field	Value	Language
dc.contributor.author	Muratov F.Kh., Yusupova D.Y	-
dc.date.accessioned	2022-12-25T17:50:07Z	-
dc.date.available	2022-12-25T17:50:07Z	-
dc.date.issued	2022	-
dc.identifier.uri	http://repository.tma.uz/xmlui/handle/1/5530	-
dc.description.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.	en_US
dc.language.iso	other	en_US
dc.publisher	ФУНДАМЕНТАЛ ВА КЛИНИК ТИББИЁТ АХБОРОТНОМАСИ	en_US
dc.title	GENETIC MARKERS OF CATAMENIAL EPILEPSY IN WOMEN	en_US
dc.type	Thesis	en_US
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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