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dc.contributor.authorPrasad, Sandhir B
dc.contributor.authorAtherton, John J
dc.date.accessioned2021-07-08T05:47:37Z
dc.date.available2021-07-08T05:47:37Z
dc.date.issued2021
dc.identifier.issn0140-6736
dc.identifier.doi10.1016/S0140-6736(21)00898-9
dc.identifier.urihttp://hdl.handle.net/10072/405848
dc.description.abstractIncreasing clinician awareness, earlier diagnosis, and implantable cardioverter-defibrillators have allowed hypertrophic cardiomyopathy to transition from being a relatively common cause of sudden death in young people to a chronic disease affecting middle-aged and older people. Mechanistic understanding of hypertrophic cardiomyopathy has been informed by elegant gene discovery studies identifying pathogenic variants in genes encoding contractile proteins, which has led to the definition of disease of the sarcomere. However, until the development of mavacamten, this definition was not accompanied by disease-specific therapies.
dc.languageeng
dc.publisherElsevier BV
dc.relation.ispartofpagefrom2440
dc.relation.ispartofpageto2441
dc.relation.ispartofissue10293
dc.relation.ispartofjournalLancet
dc.relation.ispartofvolume397
dc.subject.fieldofresearchBiomedical and clinical sciences
dc.subject.fieldofresearchCardiovascular medicine and haematology
dc.subject.fieldofresearchCardiology (incl. cardiovascular diseases)
dc.subject.fieldofresearchcode32
dc.subject.fieldofresearchcode3201
dc.subject.fieldofresearchcode320101
dc.titleQuality first in obstructive hypertrophic cardiomyopathy
dc.typeJournal article
dc.type.descriptionC3 - Articles (Letter/ Note)
dcterms.bibliographicCitationPrasad, SB; Atherton, JJ, Quality first in obstructive hypertrophic cardiomyopathy., Lancet, 2021, 397 (10293), pp. 2440-2441
dcterms.dateAccepted2021-04-09
dc.date.updated2021-07-08T04:11:53Z
gro.hasfulltextNo Full Text
gro.griffith.authorPrasad, Sandhir B.


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