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...
Main Authors: | , , , , |
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格式: | Article |
語言: | English |
出版: |
Public Library of Science (PLoS)
2009-01-01
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叢編: | PLoS ONE |
在線閱讀: | http://europepmc.org/articles/PMC2738965?pdf=render |