A 14-year-old in heart failure with multiple cardiomyopathy variants illustrates a role for signal-to-noise analysis in gene test re-interpretation.

dc.contributor.author

Connell, Patrick S

dc.contributor.author

Jeewa, Aamir

dc.contributor.author

Kearney, Debra L

dc.contributor.author

Tunuguntla, Hari

dc.contributor.author

Denfield, Susan W

dc.contributor.author

Allen, Hugh D

dc.contributor.author

Landstrom, Andrew P

dc.date.accessioned

2020-04-01T13:30:11Z

dc.date.available

2020-04-01T13:30:11Z

dc.date.issued

2019-01

dc.date.updated

2020-04-01T13:30:09Z

dc.description.abstract

Variants of unknown significance in cardiomyopathic disease should be analyzed systematically based on the prevalence of the variant in the population compared to prevalence of disease, evidence that other variants in the gene are pathologic, consistency of prediction software on pathogenicity, and the current clinical consensus.

dc.identifier

CCR31920

dc.identifier.issn

2050-0904

dc.identifier.issn

2050-0904

dc.identifier.uri

https://hdl.handle.net/10161/20302

dc.language

eng

dc.publisher

Wiley

dc.relation.ispartof

Clinical case reports

dc.relation.isversionof

10.1002/ccr3.1920

dc.subject

cardiomyopathy

dc.subject

genetic testing

dc.subject

variant of unknown significance

dc.subject

whole exome sequencing

dc.title

A 14-year-old in heart failure with multiple cardiomyopathy variants illustrates a role for signal-to-noise analysis in gene test re-interpretation.

dc.type

Journal article

duke.contributor.orcid

Landstrom, Andrew P|0000-0002-1878-9631

pubs.begin-page

211

pubs.end-page

217

pubs.issue

1

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.publication-status

Published

pubs.volume

7

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