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  • Anne-Sophie Jannot, Roubila Meziani, +15 authors Melan-Cohort
  • Medicine, Biology
  • European Journal of Human Genetics
  • 2005 (First Publication: 1 August 2005)
  • The occuloalbinism 2 (OCA2) gene, localized at 15q11, encodes a melanosomal transmembrane protein that is involved in the most common form of human occulo-cutaneous albinism, a human genetic disorderContinue Reading