A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism.

Lignende værker

• Detection of heterozygotes for tyrosinase-negative oculocutaneous albinism by hairbulb tyrosinase assay.
  af: King, R A, et al.
  Udgivet: (1977)
• Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.
  af: Spritz, R A, et al.
  Udgivet: (1991)
• A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico.
  af: Oetting, W S, et al.
  Udgivet: (1993)
• A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism.
  af: Giebel, L B, et al.
  Udgivet: (1991)
• Molecular analyses of a tyrosinase-negative albino family.
  af: Park, K C, et al.
  Udgivet: (1993)