Haematopoietic and immune defects associated with GATA2 mutation

Heterozygous familial or sporadic GATA2 mutations cause a multifaceted disorder, encompassing susceptibility to infection, pulmonary dysfunction, autoimmunity, lymphoedema and malignancy. Although often healthy in childhood, carriers of defective GATA2 alleles develop progressive loss of mononuclear...

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Detalles Bibliográficos
Autores principales: Collin, Matthew, Dickinson, Rachel, Bigley, Venetia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409096/
https://www.ncbi.nlm.nih.gov/pubmed/25707267
http://dx.doi.org/10.1111/bjh.13317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409096/
https://www.ncbi.nlm.nih.gov/pubmed/25707267
http://dx.doi.org/10.1111/bjh.13317

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