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Please use this identifier to cite or link to this item: http://tdudspace.texicon.in:8080/jspui/handle/123456789/599
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dc.contributor.authorJain, Pratul Kumar-
dc.contributor.authorDhandapany, Perundurai S-
dc.contributor.authorPalakodeti, Dasaradhi-
dc.contributor.authorJayappa, Shashank-
dc.contributor.authorSairam, Thiagarajan-
dc.date.accessioned2025-03-13T06:42:39Z-
dc.date.available2025-03-13T06:42:39Z-
dc.date.issued2021-11-
dc.identifier.urihttp://tdudspace.texicon.in:8080/jspui/handle/123456789/599-
dc.description.abstractHypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease with preserved or increased ejection fraction in the absence of secondary causes. Mutations in the sarcomeric protein-encoding genes predominantly cause HCM. However, relatively little is known about the genetic impact of signalling proteins on HCM.en_US
dc.language.isoenen_US
dc.publisherBMJ Publishing Groupen_US
dc.subjectHypertrophic cardiomyopathyen_US
dc.subjectgeneticen_US
dc.subjectHearten_US
dc.subjectRibosomal protein S6 kinase beta-1en_US
dc.subjectRPS6KB1en_US
dc.subjectS6K1en_US
dc.titleRibosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathyen_US
dc.typeArticleen_US
Appears in Collections:Researcher/Student Publications

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