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”

Παρόμοια τεκμήρια

• A hypertrophic and dilated cardiomyopathic sudden cardiac death case; de novo mutations in TTN and SGCD genes
  ανά: Baydar, Çetin Lütfi, κ.ά.
  Έκδοση: (2016)
• The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease
  ανά: Temel, Şehime Gülsün, κ.ά.
  Έκδοση: (2019)
• Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann–Rautenstrauch syndrome
  ανά: Temel, Sehime Gulsun, κ.ά.
  Έκδοση: (2020)
• A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype
  ανά: Tuncel, Gulten, κ.ά.
  Έκδοση: (2021)
• Structural and protein interaction effects of hypertrophic and dilated cardiomyopathic mutations in alpha-tropomyosin
  ανά: Chang, Audrey N., κ.ά.
  Έκδοση: (2014)