Mutations of the PEX regulatory and C-terminal regions cause X-linked hypophosphataemia.

Những quyển sách tương tự

• Seven novel mutations in the PEX gene indicate molecular heterogeneity for X-linked hypophosphataemic rickets.
  Bằng: Dixon, P, et al.
  Được phát hành: (1996)
• X-linked hypophosphataemic rickets in a Saudi Arabian kindred results from a nonsense mutation of the PEX gene.
  Bằng: Dixon, P, et al.
  Được phát hành: (1997)
• X-linked hypophosphatemia candidate gene region: Sequence data on 80 KB containing spermine synthase and the 5' region of PEX
  Bằng: Grieff, M, et al.
  Được phát hành: (1996)
• Mutational analysis of PHEX gene in X-linked hypophosphatemia.
  Bằng: Dixon, P, et al.
  Được phát hành: (1998)
• X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype
  Bằng: Whyte, M, et al.
  Được phát hành: (1999)