Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations.

Παρόμοια τεκμήρια

• A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions.
  ανά: Gehmlich, K, κ.ά.
  Έκδοση: (2011)
• Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele.
  ανά: Gehmlich, K, κ.ά.
  Έκδοση: (2012)
• Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?
  ανά: Gehmlich, K, κ.ά.
  Έκδοση: (2010)
• Genetics of and pathogenic mechanisms in arrhythmogenic right ventricular cardiomyopathy
  ανά: Vimalanathan, A, κ.ά.
  Έκδοση: (2018)
• Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro
  ανά: Beffagna, G, κ.ά.
  Έκδοση: (2007)