Human genetics study identifies the most common cause of ALS and dementia
Wednesday, September 21, 2011 - 13:30
in Biology & Nature
Scientists have made an exciting breakthrough in unraveling the genetic basis of two debilitating neurodegenerative disorders, amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Two independent studies identify a new human genetic mutation as the most common cause of ALS and FTD identified to date.