The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.

Ítems similars

• An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids.
  per: Stevens, G, et al.
  Publicat: (1995)
• The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.
  per: Ramsay, M, et al.
  Publicat: (1992)
• In Southern Africa, Brown Oculocutaneous Albinism (BOCA) Maps to the OCA2 Locus on Chromosome 15q: P-Gene Mutations Identified
  per: Manga, Prashiela, et al.
  Publicat: (2001)
• Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.
  per: Manga, P, et al.
  Publicat: (1997)
• Detection of heterozygotes for tyrosinase-negative oculocutaneous albinism by hairbulb tyrosinase assay.
  per: King, R A, et al.
  Publicat: (1977)