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Rare Neurodegenerative Diseases

European Human Genetics Conference - 2019

We have presented two posters at the European Human Genetics Conference held in Gothenburg, Sweden (June 15-18, 2019) related to the projects on the genetics of NBIA disorders, and the pathophysiology of CMT2Z. And since we were in Sweden, we had a meeting with Roman Chrast’s group at Karolinska Institutet in order to discuss the latest results of the on-going project on CMT2Z funded by the AFM Téléthon focused.