Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis
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A large-scale genetic analysis has identified new rare variant contributions to amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND). The study may have found a genetic cause for a significant portion of MND patients, although the exact proportion is not consistently reported. The discovery of these rare gene variants could potentially provide a starting point for new treatments for ALS.
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