Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinism.

Схожие документы

• A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.
  по: Giebel, L B, et al.
  Опубликовано: (1990)
• A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism.
  по: Giebel, L B, et al.
  Опубликовано: (1991)
• Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.
  по: Spritz, R A, et al.
  Опубликовано: (1991)
• Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA).
  по: Tripathi, R K, et al.
  Опубликовано: (1993)
• A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse.
  по: Giebel, L B, et al.
  Опубликовано: (1991)