Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.

समान संसाधन

• An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids.
  द्वारा: Stevens, G, और अन्य
  प्रकाशित: (1995)
• In Southern Africa, Brown Oculocutaneous Albinism (BOCA) Maps to the OCA2 Locus on Chromosome 15q: P-Gene Mutations Identified
  द्वारा: Manga, Prashiela, और अन्य
  प्रकाशित: (2001)
• The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.
  द्वारा: Kedda, M. A., और अन्य
  प्रकाशित: (1994)
• The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.
  द्वारा: Ramsay, M, और अन्य
  प्रकाशित: (1992)
• Genetic Causes of Oculocutaneous Albinism in Pakistani Population
  द्वारा: Sajid, Zureesha, और अन्य
  प्रकाशित: (2021)