Recurrent nonsense mutations in the growth hormone receptor from patients with Laron dwarfism.

Lignende værker

• Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome.
  af: Duquesnoy, P, et al.
  Udgivet: (1991)
• Lack of hormone binding in COS-7 cells expressing a mutated growth hormone receptor found in Laron dwarfism.
  af: Edery, M, et al.
  Udgivet: (1993)
• Absence of serum growth hormone binding protein in patients with growth hormone receptor deficiency (Laron dwarfism).
  af: Daughaday, W H, et al.
  Udgivet: (1987)
• Diverse growth hormone receptor gene mutations in Laron syndrome.
  af: Berg, M A, et al.
  Udgivet: (1993)
• Alternatively spliced forms in the cytoplasmic domain of the human growth hormone (GH) receptor regulate its ability to generate a soluble GH-binding protein.
  af: Dastot, F, et al.
  Udgivet: (1996)