Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene

  • Farah Ouechtati, Ahlem Merdassi, Yosra Bouyacoub, Leila Largueche, Kaouther Derouiche, Houyem Ouragini, Sonia Nouira, Leila Tiab, Karim Baklouti, Ahmed Rebai, Daniel F Schorderet, Francis L Munier, Leonidas Zografos, Sonia Abdelhak, Leila El Matri
  • Journal of Human Genetics, November 2010, Springer Science + Business Media
  • DOI: 10.1038/jhg.2010.128

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The following have contributed to this page: Dr Ahmed Rebai