Association

THE MITOFUSIN 2 ETS PROJECT ASSOCIATION was founded on 28 August 2012 by a group of relatives and friends of patients, adults and children, affected by a very rare disease: hereditary peripheral neuropathy due to mutation of the Mitofusin 2 (MFN2) gene.

The non-profit association aims to put Italian and foreign families in contact with patients affected by CMT2A, to build a continuous dialogue with researchers and clinicians (also with the support of the website) by disseminating the scientific information drawn up to by the Department of Neurological Sciences of the University of Milan directed by prof. Nereo Bresolin, to raise funds entirely intended for scientific research on the rare disease CMT2A.

In this section you can find all the documents relating to the MITOFUSINA 2 PROJECT ASSOCIATION.

Join us

We need all of you, families and already diagnosed patients, to form a large group, with a strong voice that reaches researchers and pharmaceutical companies. Join our association to get together towards the cure. Signing up is very simple!

For how to register patients, families, friends and supporters you can:

Support us

Find out how to contribute to our great project.

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