X-linked severe combined immunodeficiency disease and the gamma c receptor component: prospects for molecular diagnosis.

Documenti analoghi

• X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings.
  di: Conley, M E, et al.
  Pubblicazione: (1990)
• Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiency.
  di: Pepper, A E, et al.
  Pubblicazione: (1995)
• Lymphedema in patients with X-linked severe combined immunodeficiency
  di: Filippo Consonni, MD, et al.
  Pubblicazione: (2026-01-01)
• Severe combined immunodeficiency—molecular pathogenesis and diagnosis
  di: Gaspar, H, et al.
  Pubblicazione: (2001)
• Shared gamma(c) subunit within the human interleukin-7 receptor complex. A molecular basis for the pathogenesis of X-linked severe combined immunodeficiency.
  di: Lai, S Y, et al.
  Pubblicazione: (1997)