Source: University of Florida
Date June 8, 2009
Summary:
GAINESVILLE, Fla. — University of Florida scientists have discovered why a paralyzing brain disorder speeds along more rapidly in some patients than others — a finding that may finally give researchers an entry point toward an effective treatment for amyotrophic lateral sclerosis, often referred to as ALS or Lou Gehrig’s disease. Of more than 100 possible mutations of a single gene inherited by people with familial ALS, the mutations most inclined to produce clumps of problematic cellular debris known as “protein aggregates” appear to be associated with quicker progress of the disease, according to researchers with the University of Florida’s McKnight Brain Institute writing online this week in Human Molecular Genetics.
