An Apal RFLP for the human porphobilinogen deaminase gene (PBGD)

Míreanna comhchosúla

• An Apal RFLP for the human porphobilinogen deaminase gene (PBGD)
  de réir: Hamabe, J., et al.
  Foilsithe / Cruthaithe: (1991)
• PCR detection of a G/T polymorphism at exon 10 of the porphobilinogen deaminase gene (PBG-D).
  de réir: Gu, X F, et al.
  Foilsithe / Cruthaithe: (1991)
• A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria.
  de réir: Grandchamp, B, et al.
  Foilsithe / Cruthaithe: (1989)
• Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria.
  de réir: Delfau, M H, et al.
  Foilsithe / Cruthaithe: (1990)
• A PstI polymorphism for the human porphobilinogen deaminase gene (PBG).
  de réir: Lee, J S, et al.
  Foilsithe / Cruthaithe: (1987)