Progetto Mitofusina 2
Progetto Mitofusina 2

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Description

Association of patients with peripheral neuropathy due to mutation of gene mitofusin 2.

The aim is to find the therapy for the rare disease Charcot-Marie Tooth type 2A (CMT2A) (HMSN2A) in collaboration with Milan University.

We look for patients in Italy and all over the world to create a great group interesting for researchers and Pharmaceutical Industry.

Our website contains all informations about the disease, research on mitofusin2 and our stories and activities. We have also the database of mitofusin2 mutations.