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ISSN 2574-8300

71. Clinical Utility of a Phenotype-Enhanced MYH7-Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic Testing. (October 2020)

Authors:
Mattivi, Connor L.; Bos, J. Martijn; Bagnall, Richard D.; Nowak, Natalie; Giudicessi, John R.; Ommen, Steve R.; Semsarian, Christopher; Ackerman, Michael J.
Journal:
Circulation
Issue:
Volume 13:Number 5(2020)
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Journal Article
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76. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. (May 2018)

Authors:
Lin, Honghuang; van Setten, Jessica; Smith, Albert V.; Bihlmeyer, Nathan A.; Warren, Helen R.; Brody, Jennifer A.; Radmanesh, Farid; Hall, Leanne; Grarup, Niels; Müller-Nurasyid, Martina; Boutin, Thibaud; Verweij, Niek; Lin, Henry J.; Li-Gao, Ruifang; van den Berg, Marten E.; Marten, Jonathan; We...
Journal:
Circulation
Issue:
Volume 11:Number 5(2018)
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Record Type:
Journal Article
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77. Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction. (May 2018)

Authors:
Macri, Vincenzo; Brody, Jennifer A.; Arking, Dan E.; Hucker, William J.; Yin, Xiaoyan; Lin, Honghuang; Mills, Robert W.; Sinner, Moritz F.; Lubitz, Steven A.; Liu, Ching-Ti; Morrison, Alanna C.; Alonso, Alvaro; Li, Ning; Fedorov, Vadim V.; Janssen, Paul M.; Bis, Joshua C.; Heckbert, Susan R.; Dol...
Journal:
Circulation
Issue:
Volume 11:Number 5(2018)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗