Lowe syndrome patient fibroblasts display Ocrl1-specific...

Human Molecular Genetics 2009 / 12 Vol. 18; Iss. 23

Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase

Coon, B. G., Mukherjee, D., Hanna, C. B., Riese, D. J., Lowe, M., Aguilar, R. C.
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Volume:
18
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddp407
Date:
December, 2009
File:
PDF, 607 KB
english, 2009
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