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Identification of <i>MYOM2</i> as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot and its functional evaluation in the <i>Drosophila</i> heart

2020-08-23

Abstract excerpt

<h4>ABSTRACT</h4> The causal genetic underpinnings of congenital heart diseases, which are often complex and with multigenic background, are still far from understood. Moreover, there are also predominantly monogenic heart defects, such as cardiomyopathies, with known disease genes for the majority of cases. In this study, we identified mutations in myomesin 2 ( MYOM2 ) in patients with Tetralogy of Fallot (TOF)...

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Literature Corpus work
0959b921-11aa-5200-ab6b-f9c09dbf23ab
DOI
10.1101/2020.08.18.255760
Open publication

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Identification of <i>MYOM2</i> as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot and its functional evaluation in the <i>Drosophila</i> heartDOI 10.1101/2020.08.18.255760
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