Deletions of specific exons of FHOD3 detected by next‐generation sequencing are associated with hypertrophic cardiomyopathy

Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy

(2019) Roddy Walsh et al.   Genome Medicine

Revisiting Genome Sequencing Data in Light of Novel Disease Gene Associations

(2019) Christopher Semsarian et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy

(2018) Juan Pablo Ochoa et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

The actin-organizing formin protein Fhod3 is required for postnatal development and functional maintenance of the adult heart in mice

(2017) Tomoki Ushijima et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy

(2017) Irene Mademont-Soler et al.   PLoS One

Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy

(2015) L.R. Lopes et al.   European Journal of Medical Genetics

The Human Formin FHOD1 Contains a Bipartite Structure of FH3 and GTPase-Binding Domains Required for Activation

(2008) Antje Schulte et al.   STRUCTURE