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Differential Clathrin Binding and Subcellular Localization of OCRL1 Splice Isoforms
Mutation of the inositol polyphosphate 5-phosphatase OCRL1 causes the X-linked disorder oculocerebrorenal syndrome of Lowe, characterized by defects in the brain, kidneys, and eyes. OCRL1 exists as two splice isoforms that differ by a single exon encoding 8 amino acids. The longer protein, termed is...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Biochemistry and Molecular Biology
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2665120/ https://ncbi.nlm.nih.gov/pubmed/19211563 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M807442200 |
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