Mutation Clinical Trial
Official title:
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism
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.
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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