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Single Center Experience With Pediatric Patients With GATA2 Deficiency

GATA2 deficiency is one of the most common predisposing conditions for MDS in young individuals. It is characterized by autosomal dominant inheritance and a high rate of de novo mutations. Here we describe the clinical phenotype and hematological presentation of 10 pediatric patients with GATA2 defi...

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Detalles Bibliográficos
Autores principales: Ovsyannikova, Galina, Pavlova, Anna, Deordieva, Ekaterina, Raykina, Elena, Pshonkin, Alexey, Maschan, Alexey, Maschan, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901576/
https://www.ncbi.nlm.nih.gov/pubmed/35273927
http://dx.doi.org/10.3389/fped.2022.801810

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