Rare Things Being Common: Implications for Common Genetic Variants in Rare Diseases Like Long-QT Syndrome.

dc.contributor.author	Landstrom, Andrew P
dc.contributor.author	Shah, Svati H
dc.date.accessioned	2020-12-27T20:16:30Z
dc.date.available	2020-12-27T20:16:30Z
dc.date.issued	2020-07-27
dc.date.updated	2020-12-27T20:16:29Z
dc.identifier.issn	0009-7322
dc.identifier.issn	1524-4539
dc.identifier.uri	https://hdl.handle.net/10161/21937
dc.language	eng
dc.publisher	Ovid Technologies (Wolters Kluwer Health)
dc.relation.ispartof	Circulation
dc.relation.isversionof	10.1161/circulationaha.120.048339
dc.subject	Editorials
dc.subject	genome-wide association study
dc.subject	long QT syndrome
dc.subject	quantitative trait, heritable
dc.title	Rare Things Being Common: Implications for Common Genetic Variants in Rare Diseases Like Long-QT Syndrome.
dc.type	Journal article
duke.contributor.orcid	Landstrom, Andrew P\|0000-0002-1878-9631
duke.contributor.orcid	Shah, Svati H\|0000-0002-3495-2830
pubs.begin-page	339
pubs.end-page	341
pubs.issue	4
pubs.organisational-group	School of Medicine
pubs.organisational-group	Cell Biology
pubs.organisational-group	Pediatrics, Cardiology
pubs.organisational-group	Duke
pubs.organisational-group	Basic Science Departments
pubs.organisational-group	Pediatrics
pubs.organisational-group	Clinical Science Departments
pubs.organisational-group	Duke Clinical Research Institute
pubs.organisational-group	Duke Molecular Physiology Institute
pubs.organisational-group	Medicine, Cardiology
pubs.organisational-group	Institutes and Centers
pubs.organisational-group	Medicine
pubs.publication-status	Published
pubs.volume	142

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