Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene - Concepedia

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Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene

DOI Full Paper Access

42

Citations

27

References

2006

Year

L. El Matri, Aude Ambresin, Daniel F. Schorderet, Aki Kawasaki, Mathias W. Seeliger, Andreas Wenzel, Yvan Arsenijévic, François‐Xavier Borruat, Francis L. Munier

Graefe s Archive for Clinical and Experimental Ophthalmology

Consanguineous Tunisian FamiliesRpe65 GeneRetinaOphthalmologyOcular DiseaseGenetic DisorderGeneticsEarly-onset Retinal DegenerationMolecular GeneticsRetinal TherapiesMedicine

References

	Year	Citations

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