PCR detection of a G/T polymorphism at exon 10 of the porphobilinogen deaminase gene (PBG-D).

Benzer Materyaller

• PCR detection of a C/T polymorphism in exon 1 of the porphobilinogen deaminase gene (PBGD)
  Yazar:: Picat, C., ve diğerleri
  Baskı/Yayın Bilgisi: (1991)
• A PstI polymorphism for the human porphobilinogen deaminase gene (PBG).
  Yazar:: Lee, J S, ve diğerleri
  Baskı/Yayın Bilgisi: (1987)
• Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria.
  Yazar:: Delfau, M H, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyria.
  Yazar:: Gu, X F, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria.
  Yazar:: Grandchamp, B, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)