Gene mutation linked to hereditary spastic paraplegia has been discovered by The Scripps Research Institute (TSRI) scientists. Hereditary spastic paraplegia is a disabling neurological disorder, interferes with the normal breakdown of triglyceride fat molecules in the brain. The TSRI researchers found large droplets of triglycerides within the neurons of mice modeling the disease. The findings, reported this week online ahead of print by the journal iProceedings ...
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