Non-hereditary mutation acts as natural gene therapy in patient with rare disease

(Funda ç ã o de Amparo à Pesquisa do Estado de S ã o Paulo) Scientists at a research center supported by FAPESP identified a non-inherited mutation in blood cells from a patient with GATA2 deficiency that may have prevented bone marrow failure and other clinical manifestations.
Source: EurekAlert! - Social and Behavioral Science - Category: International Medicine & Public Health Source Type: news