Screening mutation in RYR2 gene in a Kazakhstani idiopathic ventricular tachycardia study cohort: two novel mutations

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dc.contributor.authorAkilzhanova, A.
dc.contributor.authorGuelly, C.
dc.contributor.authorAbilova, Z. M.
dc.contributor.authorRakhimova, S.
dc.contributor.authorNuralinov, O. M.
dc.contributor.authorAbdrakhmanov, A. C.
dc.contributor.authorBekbosynova, M. S.
dc.date.accessioned2015-10-22T10:57:00Z
dc.date.available2015-10-22T10:57:00Z
dc.date.issued2014
dc.description.abstractThe human ryanodine receptor 2 (RYR2) is one of the key players tightly regulating calcium efflux from the sarcoplasmic reticulum to the cytosol and found frequently mutated (<60%) in context of catecholaminergic polymorphic ventricular tachycardia (CPVT1) [1].ru_RU
dc.identifier.urihttp://nur.nu.edu.kz/handle/123456789/420
dc.language.isoenru_RU
dc.publisherNazarbayev Universityru_RU
dc.subjectventricular tachycardiaru_RU
dc.subjectventricular arrhythmiaru_RU
dc.subjectRYR2 generu_RU
dc.titleScreening mutation in RYR2 gene in a Kazakhstani idiopathic ventricular tachycardia study cohort: two novel mutationsru_RU
dc.typeAbstractru_RU

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