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Genetic Analysis of Oculocerebrorenal Syndrome of Lowe
This study has been completed.
Study NCT00359515   Information provided by National Institutes of Health Clinical Center (CC)
First Received: August 1, 2006   Last Updated: February 4, 2009   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Lowe Syndrome
Additional conditions recognized in this trial
Oculocerebrorenal Syndrome
Syndrome
More general conditions related to this trial
Abnormalities, Multiple
Amino Acid Transport Disorders, Inborn
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Central Nervous System Diseases
Congenital Abnormalities
Disease
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Kidney Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Nervous System Diseases
Pathologic Processes
Renal Tubular Transport, Inborn Errors
Urologic Diseases
Sponsors listed in this trial
National Human Genome Research Institute (NHGRI)


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