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- W1570315037 abstract "Oculocerebrorenal syndrome of Lowe (OCRL) is an X‐linked disorder with the hallmark features of congenital cataracts, mental retardation and Fanconi syndrome of the kidney proximal tubules. OCRL was first described in 1952, and exactly four decades later, the gene responsible was identified and found to encode a protein highly homologous to inositol polyphosphate 5‐phosphatase. This suggested that Lowe syndrome may represent an inborn error of inositol phosphate metabolism, and subsequent studies confirmed that such metabolism is indeed perturbed in Lowe syndrome cells. However, the mechanism by which loss of function of the OCRL1 protein brings about Lowe syndrome remains ill defined. In this review, I will discuss our understanding of OCRL1, including where it is localized, what it interacts with and what its possible functions might be. I will then discuss possible mechanisms by which loss of OCRL1 may bring about cellular defects that manifest themselves in the pathology of Lowe syndrome." @default.
- W1570315037 created "2016-06-24" @default.
- W1570315037 creator A5010533721 @default.
- W1570315037 date "2005-06-09" @default.
- W1570315037 modified "2023-10-16" @default.
- W1570315037 title "Structure and Function of the Lowe Syndrome Protein OCRL1" @default.
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- W1570315037 doi "https://doi.org/10.1111/j.1600-0854.2005.00311.x" @default.
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