July 20, 2017 connie dello buono Genomics health news Rare Gut Condition Linked to Single Gene Mutations, Hyperactivation of Complement System An exome sequencing analysis of individuals from eight families led to homozygous loss-of-function mutations in CD55 and ties to complement system activity. Read more > Single Gene Mutations Implicated in New Intellectual Disability Syndrome Mutations in the WDR26 gene appear to contribute to a condition marked by intellectual disability, facial dysmorphism, and movement problems. Read more > WUSTL Team Develops Blood-Based Test for Brain Amyloidosis The test, which measures the kinetics of amyloid beta isoforms in blood, could enable more efficient screening of patients for Alzheimer’s drug trials. Read more > Share this:TwitterFacebookLinkedInPrintEmailGooglePocketPinterestTumblrRedditLike this:Like Loading...
