GATA2突变相关儿童原发性骨髓增生异常综合征临床及分子生物学特征

OBJECTIVE: To clarify the prevalence, clinical features and molecular characteristics of germline GATA2 mutations in pediatric primary myelodysplastic syndromes (MDS). METHODS: Next-generation sequencing technology was used to detect mutations in GATA2 and other myeloid malignancy genes in 129 child...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
论著
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342394/
https://www.ncbi.nlm.nih.gov/pubmed/31340620
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342394/
https://www.ncbi.nlm.nih.gov/pubmed/31340620
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.006

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