Disruption of cytoskeleton pathways contribute to amyotrophic lateral sclerosis pathogenesis
09:14 EDT 15 Jul 2012 | Science Daily
A new genetic mutation that causes familial amyotrophic lateral sclerosis (ALS), a fatal neurological disorder also known as Lou Gehrig's Disease, has been identified. Mutations to the profilin gene, which is essential to the growth and development o..
Original Article: Disruption of cytoskeleton pathways contribute to amyotrophic lateral sclerosis pathogenesis
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