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Stanley Manne Children's Research Institute



New gene variant identified in ALS provides treatment hope

17 May 2017 | By

A new study shows that a variant in UBQLN4 gene has been associated with Lou Gehrig's disease, or amyotrophic lateral sclerosis (ALS). The study also describes how this gene variant disrupts a cellular process that drives motor neuron development. This new insight opens the door to potential treatment targets for…