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Clinical Trial Summary

The oculocutaneous albinism is an autosomal recessive condition associated with mutations in 4 genes. In 20% of patients no mutation is identified. The optimization of genetic analysis methods and the search for new genes involved will help improve the diagnosis in these patients.


Clinical Trial Description

The oculocutaneous albinism is an autosomal recessive condition associated with mutations in 4 genes. In 20% of patients no mutation is identified. The optimization of genetic analysis methods and the search for new genes involved will help improve the diagnosis in these patients.

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Study Design


Related Conditions & MeSH terms


NCT number NCT04068961
Study type Observational
Source University Hospital, Bordeaux
Contact
Status Completed
Phase
Start date September 15, 2010
Completion date October 31, 2010

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