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VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesis.

Ariane LunatiArnaud PetitHélène LapillonneChristine GameiroVirginie SaillourCatherine GarelDiane DoummarLeila QebiboAbdelrazak AissatPascale FanenPablo BartolucciFréderic GalactérosBenoit FunalotLydie BurglenLamisse Mansour-Hendili
Published in: American journal of hematology (2021)
Keyphrases
  • intellectual disability
  • iron deficiency
  • chronic kidney disease
  • autism spectrum disorder