Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation with new clinical features: a case report

Lignende værker

• Large Deletions and Point Mutations Involving DOCK8 in the Autosomal Recessive Form of the Hyper-IgE Syndrome
  af: Engelhardt, Karin R., et al.
  Udgivet: (2009)
• Autosomal-Recessive Hyper-IgE Syndrome
  af: Liza, Mohapatra, et al.
  Udgivet: (2018)
• Deficient T Cell Receptor Excision Circles (TRECs) in Autosomal Recessive Hyper IgE Syndrome Caused by DOCK8 Mutation: Implications for pathogenesis and potential detection by newborn screening
  af: Dasouki, Majed, et al.
  Udgivet: (2011)
• Successful engraftment of donor marrow following allogeneic hematopoietic cell transplantation in autosomal recessive Hyper IgE syndrome due to DOCK8 deficiency
  af: McDonald, Douglas R., et al.
  Udgivet: (2010)
• Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
  af: Hagl, Beate, et al.
  Udgivet: (2018)