COL6A1 loss of function mutation underlie atrioventricular septal defects in down syndrome patients

Παρόμοια τεκμήρια

• An intronic rare mutation in Presenilin-1 (PSEN-1) gene may be involved in the developement of Alzheimer’s disease
  ανά: Bhaumik, Pranami, κ.ά.
  Έκδοση: (2014)
• Atrioventricular Septal Defects
  ανά: Chauhan, Sandeep
  Έκδοση: (2018)
• Combined association of Presenilin-1 and Apolipoprotein E polymorphisms with maternal meiosis II error in Down syndrome births
  ανά: Bhaumik, Pranami, κ.ά.
  Έκδοση: (2017)
• Improvement of surgical outcomes of complete atrioventricular septal defect with Tetralogy of Fallot
  ανά: Morimoto, K
  Έκδοση: (2013)
• Recent advances in managing septal defects: ventricular septal defects and atrioventricular septal defects
  ανά: Rao, P Syamasundar, κ.ά.
  Έκδοση: (2018)