SYDNEY, Sept. 11 (Xinhua) -- Researchers in Australia have developed a genome editing approach that could provide a more durable treatment for children with a rare genetic liver disorder. Researchers have taken an important step toward overcoming a key challenge in gene therapy for children with metabolic liver disorders: the liver's growth can gradually dilute the treatment as new, untreated cells emerge, accor
Gene editing approach could provide lasting treatment for rare liver disease: study
