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SBDS Expression and Localization at the Mitotic Spindle in Human Myeloid Progenitors
BACKGROUND: Shwachman-Diamond Syndrome (SDS) is a hereditary disease caused by mutations in the SBDS gene. SDS is clinically characterized by pancreatic insufficiency, skeletal abnormalities and bone marrow dysfunction. The hematologic abnormalities include neutropenia, neutrophil chemotaxis defects...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2009
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| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2738965/ https://ncbi.nlm.nih.gov/pubmed/19759903 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0007084 |
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