Oculocutaneous Albinism Type 4 Is One of the Most Common Types of Albinism in Japan

This publication has 13 references indexed in Scilit:

• Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4
  American Journal of Human Genetics, 2001
• Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka
  Nature Genetics, 2001
• Use of an in vitro immunoselected tumor line to identify shared melanoma antigens recognized by HLA-A*0201-restricted T cells.
  2001
• Molecular Bases of Congenital Hypopigmentary Disorders in Humans and Oculocutaneous Albinism 1 in Japan
  Pigment Cell Research, 2000
• Brief communication. A new allelic series for the underwhite gene on mouse chromosome 15
  Journal of Heredity, 1998
• Rufous Oculocutaneous Albinism in Southern African Blacks Is Caused by Mutations in the TYRP1 Gene
  American Journal of Human Genetics, 1997
• Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".
  1996
• A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism
  Nature, 1993
• Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.
  1992
• Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene
  Biochemical and Biophysical Research Communications, 1989