Loss of OCRL increases ciliary PI(4,5)P2in Lowe oculocerebrorenal syndrome
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Title
Loss of OCRL increases ciliary PI(4,5)P2in Lowe oculocerebrorenal syndrome
Authors
Keywords
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Journal
JOURNAL OF CELL SCIENCE
Volume 130, Issue 20, Pages 3447-3454
Publisher
The Company of Biologists
Online
2017-09-05
DOI
10.1242/jcs.200857
References
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Related references
Note: Only part of the references are listed.- Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
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- Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase
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