Dergiler / The Anatolian Journal of Cardiology / 2017 / Cilt: 17 - Sayı: 1

Letter to the editor regarding the article A case of hypertrophic and dilated cardiomyopathic sudden cardiac death: de novo mutation in TTN and SGCD genes

Sayfa
76–77
DOI
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ERGÖREN, M. Ç., TEMEL, Ş. G. (2017). Letter to the editor regarding the article A case of hypertrophic and dilated cardiomyopathic sudden cardiac death: de novo mutation in TTN and SGCD genes. The Anatolian Journal of Cardiology, Cilt: 17 - Sayı: 1, 76–77. https://ajindex.com/articles/365354

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Kaynakça (2)

  1. Baydar CL, Özen M. A case of hypertrophic and dilated cardiomyopathic sudden cardiac death: de novo mutation in TTN and SGGD genes. Anatol J Cardiol 2016 Jul 31. Epub ahead of print. Veltman JA, Brunner HG. De novo mutations in human genetic disease. Nat Rev Genet 2012; 13: 565-75. http://exac.broadinstitute.org
  2. Pugh TJ, Kelly MA, Gowrisankar S, Hynes E, Seidman MA, Baxter SM, et al. The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. Genet Med 2014; 6: 601-8. General Variant Classification Assertion Criteria. GeneDx DNA Diagnostic Experts. http://www.genedx.com