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10.3389/fcvm.2018.00077 http://scihub22266oqcxt.onion/10.3389/fcvm.2018.00077 C6028572!6028572!29998127     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=29998127&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Front+Cardiovasc+Med 2018 ; 5 (ä): ä Nephropedia Template TP {{tp|p=29998127|t=2018. Inherited Cardiomyopathies and the Role of Mutations in Non-coding Regions of the Genome |pdf=|usr=}}{{29998127}} gab.com Text Inherited Cardiomyopathies and the Role of Mutations in Non-coding Regions of the Genome JO: Front Cardiovasc Med http://www.kidney.de/pget.php?&tw=1&pmid=29998127 #FOAvip Cardiomyopathies (CMs) are a group of cardiac pathologies caused by an intrinsic defect within the myocardium. The relative contribution of genetic mutations in the pathogenesis of certain CMs, such as hypertrophic cardiomyopathy (HCM), arrythmogenic right/left ventricular cardiomyopathy (ARVC) and left ventricular non-compacted cardiomyopathy (LVNC) has been established in comparison to dilated cardiomyopathy (DCM) and restrictive cardiomyopathy (RCM). The aim of this article is to review mutations in the non-coding parts of the genome, namely, microRNA, promoter elements, enhancer/silencer elements, 3?/5?UTRs and introns, that are involved in the pathogenesis CMs. Additionally, we will explore the role of some long non-coding RNAs in the pathogenesis of CMs. Twit Text FOAVip Inherited Cardiomyopathies and the Role of Mutations in Non-coding Regions of the Genome ????Front Cardiovasc Med http://www.kidney.de/pget.php?&tw=1&pmid=29998127 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29998127 #FOAvip English Wikipedia <ref>{{Cite pmid|29998127}}</ref> Inherited Cardiomyopathies and the Role of Mutations in Non-coding Regions of the Genome #MMPMID29998127 Salman OF; El-Rayess HM; Abi Khalil C; Nemer G; Refaat MM Front Cardiovasc Med 2018[]; 5 (ä): ä PMID29998127show ga Cardiomyopathies (CMs) are a group of cardiac pathologies caused by an intrinsic defect within the myocardium. The relative contribution of genetic mutations in the pathogenesis of certain CMs, such as hypertrophic cardiomyopathy (HCM), arrythmogenic right/left ventricular cardiomyopathy (ARVC) and left ventricular non-compacted cardiomyopathy (LVNC) has been established in comparison to dilated cardiomyopathy (DCM) and restrictive cardiomyopathy (RCM). The aim of this article is to review mutations in the non-coding parts of the genome, namely, microRNA, promoter elements, enhancer/silencer elements, 3?/5?UTRs and introns, that are involved in the pathogenesis CMs. Additionally, we will explore the role of some long non-coding RNAs in the pathogenesis of CMs. äInherited Cardiomyopathies and the Role of Mutations in Non-coding Reg(epmc).pdf DeepDyve Pubget Overpricing