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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.issn0140-6736en_US
dc.identifier.doi10.1016/S0140-6736(21)00898-9en_US
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.en_US
dc.languageengen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofpagefrom2440en_US
dc.relation.ispartofpageto2441en_US
dc.relation.ispartofissue10293en_US
dc.relation.ispartofjournalLanceten_US
dc.relation.ispartofvolume397en_US
dc.subject.fieldofresearchCardiology (incl. Cardiovascular Diseases)en_US
dc.subject.fieldofresearchCardiorespiratory Medicine and Haematologyen_US
dc.subject.fieldofresearchMedical and Health Sciencesen_US
dc.subject.fieldofresearchcode110201en_US
dc.subject.fieldofresearchcode1102en_US
dc.subject.fieldofresearchcode11en_US
dc.titleQuality first in obstructive hypertrophic cardiomyopathyen_US
dc.typeJournal articleen_US
dc.type.descriptionC3 - Articles (Letter/ Note)en_US
dcterms.bibliographicCitationPrasad, SB; Atherton, JJ, Quality first in obstructive hypertrophic cardiomyopathy., Lancet, 2021, 397 (10293), pp. 2440-2441en_US
dcterms.dateAccepted2021-04-09
dc.date.updated2021-07-08T04:11:53Z
gro.hasfulltextNo Full Text
gro.griffith.authorPrasad, Sandhir B.


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