Young woman with mild bone marrow dysplasia, GATA2 and ASXL1 mutation treated with allogeneic hematopoietic stem cell transplantation

Heterozygous mutations in GATA2 underlie different syndromes, previously described as monocytopenia and mycobacterial avium complex infection (MonoMAC); dendritic cell, monocytes, B- and NK lymphocytes deficiency (DCML); lymphedema, deafness and myelodysplasia (Emberger syndrome) and familiar myelod...

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Detalhes bibliográficos
Publicado no:Leuk Res Rep
Main Authors: Lübking, Anna, Vosberg, Sebastian, Konstandin, Nikola P., Dufour, Annika, Graf, Alexander, Krebs, Stefan, Blum, Helmut, Weber, Axel, Lenhoff, Stig, Ehinger, Mats, Spiekermann, Karsten, Greif, Philipp A., Cammenga, Jörg
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4672090/
https://ncbi.nlm.nih.gov/pubmed/26716079
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.lrr.2015.10.001
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