UCL News


Cot death could partly be down to genetic mutation

29 March 2018

Professor Michael Hanna (UCL Institute of Neurology) led a study finding that rare genetic mutations associated with impairment of the breathing muscles are more common in children who have died from sudden infant death syndrome. Read: The Guardian, Watch: Channel 4 NewsMore: Times (£), CNN, Washington Post, IndependentITV News, NBC, CBS, Huffington Post, UCL News