Genetic cause identified for one in four MND patients in largest ever rare variant analysis

Project MinE, an international consortium co-founded by researchers at King’s College London, has identified new genetic variants that play a role in the development of motor neuron disease (MND). These findings mean that a genetic component is identifiable for 1 in 4 people with MND, a sizable increase from previous estimates of 1 in 5.

This article was originally published on MedicalXpress.com

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