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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Detalles Bibliográficos
Autores principales: Orelio, Claudia, Verkuijlen, Paul, Geissler, Judy, van den Berg, Timo K., Kuijpers, Taco W.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2738965/
https://www.ncbi.nlm.nih.gov/pubmed/19759903
http://dx.doi.org/10.1371/journal.pone.0007084

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2738965/
https://www.ncbi.nlm.nih.gov/pubmed/19759903
http://dx.doi.org/10.1371/journal.pone.0007084

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