Identification of a point mutation in the adenosine deaminase gene responsible for immunodeficiency.

Benzer Materyaller

• Identification of a point mutation resulting in a heat-labile adenosine deaminase (ADA) in two unrelated children with partial ADA deficiency.
  Yazar:: Hirschhorn, R, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Identification of an Apa I polymorphism within the human adenosine deaminase (ADA) gene.
  Yazar:: Gribbin, T, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• One adenosine deaminase allele in a patient with severe combined immunodeficiency contains a point mutation abolishing enzyme activity.
  Yazar:: Valerio, D, ve diğerleri
  Baskı/Yayın Bilgisi: (1986)
• Adenosine deaminase: demonstration of a "silent" gene associated with combined immunodeficiency disease.
  Yazar:: Chen, S H, ve diğerleri
  Baskı/Yayın Bilgisi: (1974)
• Paradoxical expression of adenosine deaminase in T cells cultured from a patient with adenosine deaminase deficiency and combine immunodeficiency.
  Yazar:: Arredondo-Vega, F X, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)