ANXA11 – another gene closer to understanding MND
Researchers from King’s College London. Dr Bradley Smith and colleagues screened genetic data of an unusually high number of people of European origin finding that specific mutations in the ANXA11 gene are associated with around 1% of all familial ALS/MND and 1.7% of all sporadic ALS/MND cases. While this may seem like a small percentage, it is another great finding that can tell us more about the mechanisms of MND.