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Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1
Mutations of the inositol 5′ phosphatase oculocerebrorenal syndrome of Lowe (OCRL) give rise to the congenital X-linked disorders oculocerebrorenal syndrome of Lowe and Dent disease, two conditions giving rise to abnormal kidney proximal tubule reabsorption, and additional nervous system and ocular...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
National Academy of Sciences
2010
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2840420/ https://ncbi.nlm.nih.gov/pubmed/20133602 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0914658107 |
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