Aberrant glycosylation of IgA in Wiskott–Aldrich syndrome and X-linked thrombocytopenia

Samankaltaisia teoksia

• Analysis of T-cell repertoire diversity in Wiskott-Aldrich syndrome
  Tekijä: Wada, Taizo, et al.
  Julkaistu: (2005)
• Development of IgA nephropathy-like glomerulonephritis associated with Wiskott-Aldrich syndrome protein deficiency
  Tekijä: Shimizu, M, et al.
  Julkaistu: (2011)
• Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblings
  Tekijä: Wada, Taizo, et al.
  Julkaistu: (2003)
• Broad spectrum of autoantibodies in Wiskott-Aldrich Syndrome (WAS) and X-linked Thrombocytopenia (XLT)
  Tekijä: Crestani, Elena, et al.
  Julkaistu: (2015)
• Somatic mosaicism in Wiskott–Aldrich syndrome suggests in vivo reversion by a DNA slippage mechanism
  Tekijä: Wada, Taizo, et al.
  Julkaistu: (2001)