MCOPS12: joint treatment development with an international association

Syndromic microphthalmia 12 (MCOPS12) is a rare genetic disease causing microphthalmia, as well as significant motor and intellectual disorders. In collaboration with Canadian, Swiss and French scientists, supported by funds from the European Community and the Cure MCOPS12 association, Wojciech Krezel's group is studying the mechanisms of neurodegeneration in this disease, with a the aim of developing a therapeutic strategy.

See the article on the INRT website