» Published on
26. November 2021
More targeted treatment of muscular dystrophy in future
Bielefeld University researchers identify causative gene
For the targeted treatment of a disease, information is needed about the course of the disease at molecular and cellular level. This is also true for the group of muscle diseases that include congenital muscular dystrophies (CMD). Bielefeld scientists have been able to identify a crucial gene that triggers CMD when it ceases to function. The principal collaborator is the research group of Carsten G. Bönnemann, M.D., of the National Institutes of Health in the USA; numerous other international partners were involved in the research project. The collaboration is financed by third-party funds from the German Research Foundation (DFG). The results were published in the EMBO Molecular Medicine journal on 15 November 2021.
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