Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency

The human syndrome of dendritic cell, monocyte, B and natural killer lymphoid deficiency presents as a sporadic or autosomal dominant trait causing susceptibility to mycobacterial and other infections, predisposition to myelodysplasia and leukemia, and, in some cases, pulmonary alveolar proteinosis....

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Publicado en:Blood
Autores principales: Dickinson, Rachel Emma, Griffin, Helen, Bigley, Venetia, Reynard, Louise N., Hussain, Rafiqul, Haniffa, Muzlifah, Lakey, Jeremy H., Rahman, Thahira, Wang, Xiao-Nong, McGovern, Naomi, Pagan, Sarah, Cookson, Sharon, McDonald, David, Chua, Ignatius, Wallis, Jonathan, Cant, Andrew, Wright, Michael, Keavney, Bernard, Chinnery, Patrick F., Loughlin, John, Hambleton, Sophie, Santibanez-Koref, Mauro, Collin, Matthew
Formato: Artigo
Lenguaje:Inglês
Publicado: 2011
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5137783/
https://ncbi.nlm.nih.gov/pubmed/21765025
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2011-06-360313
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