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Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients
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Physical mapping and genomic structure of the Lowe syndrome gene OCRL1
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Periventricular white matter cystic lesions in Lowe (Oculocerebrorenal) syndrome: A new MR finding
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The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase
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