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GATA2 deficiency and human hematopoietic development modeled using induced pluripotent stem cells
GATA2 deficiency is an inherited or sporadic genetic disorder characterized by distinct cellular deficiency, bone marrow failure, various infections, lymphedema, pulmonary alveolar proteinosis, and predisposition to myeloid malignancies resulting from heterozygous loss-of-function mutations in the G...
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| Publicado en: | Blood Adv |
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| Main Authors: | , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
American Society of Hematology
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6290105/ https://ncbi.nlm.nih.gov/pubmed/30538114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2018017137 |
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