Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2


YÜCEL E.

The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021, İstanbul, Turkey, 10 November 2021

  • Publication Type: Conference Paper / Summary Text
  • City: İstanbul
  • Country: Turkey