Formin Homology 2 Domain Containing 3 (FHOD3) 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 g...

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Detalhes bibliográficos
Main Authors: Wooten, Eric C., Hebl, Virginia Bartleson, Wolf, Matthew J., Greytak, Sarah R., Orr, Nicole, 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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3578062/
https://ncbi.nlm.nih.gov/pubmed/23255317
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.112.965277
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