Viewing StudyNCT00359515



Ignite Creation Date: 2024-05-05 @ 4:56 PM
Last Modification Date: 2024-10-26 @ 9:26 AM
Study NCT ID: NCT00359515
Status: COMPLETED
Last Update Posted: 2017-07-02
First Post: 2006-08-01

Brief Title: Genetic Analysis of Oculocerebrorenal Syndrome of Lowe
Sponsor: National Human Genome Research Institute NHGRI
Organization: National Institutes of Health Clinical Center CC

Conditions & Keywords Data

Conditions:
Name
Lowe Syndrome
Keywords:
Name View
Genotype View
Archived Samples View
Mutation Screening View
Genotype-Phenotype Correlation View
Pediatric Developmental Disorder View
Cataracts View
Mutation Detection View
Lowe Syndrome View