(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.
Fonte/Source: https://www.eurekalert.org/pub_releases/2020-11/fda-nma111720.php
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