Heart Failure and Cardiac Disease

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Investigating the Genetic Causes of Sudden Unexpected Death in Children Through Targeted Next-Generation Sequencing AnalysisCLINICAL PERSPECTIVE
Laura J. Dewar, Miguel Alcaide, Daniel Fornika, Luisa D’Amato, Sanam Shafaatalab, Charles M. Stevens, Thambirajah Balachandra, Susan M. Phillips, Shubhayan Sanatani, Ryan D. Morin and Glen F. Tibbits

Circulation: Cardiovascular Genetics. 2017;10:e001738, originally published August 14, 2017
https://doi.org/10.1161/CIRCGENETICS.116.001738

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Fabry Disease in Families With Hypertrophic CardiomyopathyCLINICAL PERSPECTIVEClinical Manifestations in the Classic and Later-Onset Phenotypes
Berglind Adalsteinsdottir, Runolfur Palsson, Robert J. Desnick, Marianna Gardarsdottir, Polakit Teekakirikul, Martin Maron, Evan Appelbaum, Ulf Neisius, Barry J. Maron, Michael A. Burke, Brenden Chen, Silvere Pagant, Christoffer V. Madsen, Ragnar Danielsen, Reynir Arngrimsson, Ulla Feldt-Rasmussen, Jonathan G. Seidman, Christine E. Seidman and Gunnar Th. Gunnarsson

Circulation: Cardiovascular Genetics. 2017;10:e001639, originally published August 10, 2017
https://doi.org/10.1161/CIRCGENETICS.116.001639

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Fabry DiseaseA Rare Condition Emerging From the Darkness
Perry M. Elliott

Circulation: Cardiovascular Genetics. 2017;10:e001862, originally published August 10, 2017
https://doi.org/10.1161/CIRCGENETICS.117.001862

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Novel Genetic Triggers and Genotype–Phenotype Correlations in Patients With Left Ventricular NoncompactionCLINICAL PERSPECTIVE
Karol Miszalski-Jamka, John L. Jefferies, Wojciech Mazur, Jan Głowacki, Jianhong Hu, Monika Lazar, Richard A. Gibbs, Jacek Liczko, Jan Kłyś, Eric Venner, Donna M. Muzny, Jarosław Rycaj, Jacek Białkowski, Ewa Kluczewska, Zbigniew Kalarus, Shalini Jhangiani, Hussein Al-Khalidi, Tomasz Kukulski, James R. Lupski, William J. Craigen and Matthew N. Bainbridge

Circulation: Cardiovascular Genetics. 2017;10:e001763, originally published August 10, 2017
https://doi.org/10.1161/CIRCGENETICS.117.001763

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Navigating Genetic and Phenotypic Uncertainty in Left Ventricular Noncompaction
June-Wha Rhee, Megan E. Grove and Euan A. Ashley

Circulation: Cardiovascular Genetics. 2017;10:e001857, originally published August 10, 2017
https://doi.org/10.1161/CIRCGENETICS.117.001857

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Clinical Characteristics and Long-Term Outcome of Hypertrophic Cardiomyopathy in Individuals With a MYBPC3 (Myosin-Binding Protein C) Founder MutationCLINICAL PERSPECTIVE
Hannah G. van Velzen, Arend F.L. Schinkel, Rogier A. Oldenburg, Marjon A. van Slegtenhorst, Ingrid M.E. Frohn-Mulder, Jolanda van der Velden and Michelle Michels

Circulation: Cardiovascular Genetics. 2017;10:e001660, originally published August 9, 2017
https://doi.org/10.1161/CIRCGENETICS.116.001660

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Founder Mutations in Myosin-Binding Protein CMaybe Not So Benign After All
Andrea D. Thompson and Sharlene M. Day

Circulation: Cardiovascular Genetics. 2017;10:e001872, originally published August 9, 2017
https://doi.org/10.1161/CIRCGENETICS.117.001872

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Lamin A/C-Related Cardiac DiseaseCLINICAL PERSPECTIVELate Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation
Edgar T. Hoorntje, Ilse A. Bollen, Daniela Q. Barge-Schaapveld, Florence H. van Tienen, Gerard J. te Meerman, Joeri A. Jansweijer, Anthonie J. van Essen, Paul G. Volders, Alina A. Constantinescu, Peter C. van den Akker, Karin Y. van Spaendonck-Zwarts, Rogier A. Oldenburg, Carlo L. Marcelis, Jasper J. van der Smagt, Eric A. Hennekam, Aryan Vink, Marianne Bootsma, Emmelien Aten, Arthur A. Wilde, Arthur van den Wijngaard, Jos L. Broers, Jan D. Jongbloed, Jolanda van der Velden, Maarten P. van den Berg and J. Peter van Tintelen

Circulation: Cardiovascular Genetics. 2017;10:e001631, originally published August 8, 2017
https://doi.org/10.1161/CIRCGENETICS.116.001631

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LMNA Mutations Associated With Mild and Late-Onset PhenotypeThe Case of the Dutch Founder Mutation p.(Arg331Gln)
Eloisa Arbustini, Valentina Favalli and Nupoor Narula

Circulation: Cardiovascular Genetics. 2017;10:e001816, originally published August 8, 2017
https://doi.org/10.1161/CIRCGENETICS.117.001816

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Previously Unreported in Women Galactosidase Alpha Pro409Ser Variant Is Associated With Fabry Disease
Sushil Allen Luis, Joseph J. Maleszewski, Phillip M. Young, Hartzell V. Schaff and Naveen L. Pereira

Circulation: Cardiovascular Genetics. 2017;10:e001661, originally published August 2, 2017
https://doi.org/10.1161/CIRCGENETICS.116.001661

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