Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome.

Podobne zapisy

• Recurrent nonsense mutations in the growth hormone receptor from patients with Laron dwarfism.
  od: Amselem, S, i wsp.
  Wydane: (1991)
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  od: Duquesnoy, P, i wsp.
  Wydane: (1994)
• Alternatively spliced forms in the cytoplasmic domain of the human growth hormone (GH) receptor regulate its ability to generate a soluble GH-binding protein.
  od: Dastot, F, i wsp.
  Wydane: (1996)
• Primary growth hormone insensitivity (Laron syndrome) and acquired hypothyroidism: a case report
  od: Corneli Ginevra, i wsp.
  Wydane: (2011-07-01)
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  od: Cotta, Oana R, i wsp.
  Wydane: (2011)