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Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis.

Janina Schwenty-LaraAnnika NürnbergerAnnette Borchers
Published in: Developmental dynamics : an official publication of the American Association of Anatomists (2019)
Kmt2d loss of function in Xenopus recapitulates the hypoplastic heart defects observed in Kabuki syndrome patients and shows that Kmt2d function is required for the establishment of the primary and secondary heart fields. Thus, Xenopus Kmt2d morphants can be a valuable tool to elucidate the etiology of the congenital heart defects associated with Kabuki syndrome.
Keyphrases
  • heart failure
  • end stage renal disease
  • case report
  • atrial fibrillation
  • cell free
  • ejection fraction
  • chronic kidney disease
  • genome wide
  • gene expression
  • peritoneal dialysis
  • dna methylation
  • patient reported outcomes