Agenparl (Itália)

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

Publicado em 18 novembro 2020

(AGENPARL) – WORCESTER (MASSACHUSETTS), mer 18 novembre 2020 (Fundação de Amparo à Pesquisa do Estado de São 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.