Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy

BACKGROUND: Restrictive cardiomyopathy (RCM) is a rare cardiomyopathy characterized by impaired diastolic ventricular function resulting in a poor clinical prognosis. Rarely, heritable forms of RCM have been reported and mutations underlying RCM have been identified in genes that govern the contract...

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Bibliografski detalji
Izdano u:Circ Cardiovasc Genet
Glavni autori: Tucker, Nathan R., McLellan, Micheal A., Hu, Dongjian, Ye, Jiangchuan, Parsons, Victoria A., Mills, Robert W., Clauss, Sebastian, Dolmatova, Elena, Shea, Marisa A., Milan, David J., Scott, Nandita S., Lindsay, Mark, Lubitz, Steven A., Domian, Ibrahim J., Stone, James R., Lin, Honghuang, Ellinor, Patrick T.
Format: Artigo
Jezik:Inglês
Izdano: 2017
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5802346/
https://ncbi.nlm.nih.gov/pubmed/29212899
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.117.001780
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