New drugs are being developed to treat Duchenne Muscular Dystrophy — and many other rare diseases — but the treatments are stalled at the FDA. A new Kickstarter campaign is raising funds to complete a documentary about parents fighting to stop Duchenne Muscular Dystrophy and gain access to potentially life-saving drugs before the disease kills their children.
Researchers at the University of California, San Francisco, have discovered the first gene involved in regulating the length of human sleep. The study, published recently in the journal Science, identified a genetic mutation that is associated with a short human sleep phenotype . The finding may help scientists better understand the regulatory mechanisms of sleep and lead to treatments for a variety of sleep disorders.