Rufous Oculocutaneous Albinism in Southern African Blacks Is Caused by Mutations in the TYRP1 Gene

This publication has 32 references indexed in Scilit:

• Chromosomal Structure of the Human TYRP1 and TYRP2 Loci and Comparison of the Tyrosinase-Related Protein Gene Family
  Genomics, 1995
• Dinucleotide repeat polymorphism at the human TYRP1 locus
  Human Molecular Genetics, 1994
• African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism
  Nature Genetics, 1994
• Assignment of the Tyrosinase-Related Protein-2 Gene (TYRP2) to Human Chromosome 13q31-q32 by Fluorescence in Situ Hybridization: Extended Synteny with Mouse Chromosome 14
  Genomics, 1994
• An Ultrastructural Study of Melanocytes and Melanosomes in the Skin and Hair Bulbs of Rufous Albinos
  Pigment Cell Research, 1993
• Assignment of the human TYRP (brown) locus to chromosome region 9p23 by nonradioactive in situ hybridization
  Genomics, 1992
• Mapping the human CAS2 gene, the homologue of the mouse brown (b) locus, to human Chromosome 9p22-pter
  Biochemical and Biophysical Research Communications, 1991
• Red or rufous albinism in Southern Africa
  Ophthalmic Paediatrics and Genetics, 1990
• Human tyrosinase gene, mapped to chromosome 11 (q14 → q21), defines second region of homology with mouse chromosome 7
  Genomics, 1988
• A case of mutual reduction of dominance: observed in Mus musculus
  Heredity, 1953