Formin Homology 2 Domain Containing 3 Variants Associated With Hypertrophic Cardiomyopathy

BACKGROUND—Incomplete penetrance and variable expression of hypertrophic cardiomyopathy (HCM) is well appreciated. Common genetic polymorphisms variants that may affect HCM penetrance and expression have been predicted but are not well established. METHODS AND RESULTS—We performed a case-control gen...

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Veröffentlicht in:	Circulation. Cardiovascular genetics 2013-02, Vol.6 (1), p.10-18
Hauptverfasser:	Wooten, Eric C, Hebl, Virginia B, Wolf, Matthew J, Greytak, Sarah R, Orr, Nicole M, Draper, Isabelle, Calvino, Jenna E, Kapur, Navin K, Maron, Martin S, Kullo, Iftikhar J, Ommen, Steve R, Bos, J Martijn, Ackerman, Michael J, Huggins, Gordon S
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Base Sequence Cardiomyopathy, Hypertrophic - genetics Case-Control Studies Chromosomes, Human, Pair 18 - genetics Cohort Studies Female Genetic Association Studies Humans Introns Male Microfilament Proteins - genetics Middle Aged Molecular Sequence Data Polymorphism, Single Nucleotide Young Adult
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