Actualités

Identification of a new mutation affecting the IRF4 gene associated with a primary immunodeficiency

The cytoplasmic protein RIPK3 influences the severity of viral encephalitis due to herpes by limiting the viral load

Discovery of DOCK11 mutations responsible for a new X-linked autoimmune disease

Identification of a new gene involved in severe allergies and eczema

Launch of a sponsorship partnership with BNP Paribas Cardif

Identification of a whole new type of mutation in immune deficiencie

Accelerating gene therapy: assessment and prospects at the end of the DIM Gene Therapy program

Training today for better care tomorrow

Covid-19: inborn errors responsible for multisystemic inflammatory syndrome in children

A new tool to correct a mutation in beta-thalassemia

The Institut Imagine, for a human medicine focused on patients and their families

Giving to Imagine to transform the lives of children with genetic diseases

A look at the latest advances in gene therapy

A look back at the Dravet Syndrome Alliance Days

New international partnership : A vision for the future of genetic medicine services