A novel RDS/peripherin gene mutation associated with diverse macular phenotypes

By Yang Zhenglin   Li Yang   Jiang Li   Karan Goutam   Moshfeghi Darius   O'Connor Scott   Li Xi   Yu Zhengya   Lewis Hilel   Zack Donald   Jacobson Samuel   Zhang Kang  

Ophthalmic Genetics, Vol. 25, Iss. 2, 2004-06 ,pp. : 133-145

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A correlation between computer-predicted changes in secondary structure and the phenotype of retinal degeneration associated with mutations in peripherin/RDS

By Nakazawa Mitsuru   Wada Yuko   Chida Yasushi   Tamai Makoto  

Current Eye Research, Vol. 16, Iss. 11, 1997-11 ,pp. : 1134-1141

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Molecular Screening of Rhodopsin and Peripherin/RDS Genes in Mexican Families with Autosomal Dominant Retinitis Pigmentosa

By Matias-Florentino Margarita   Ayala-Ramirez Raul   Graue-Wiechers Federico   Zenteno Juan Carlos  

Current Eye Research, Vol. 34, Iss. 12, 2009-12 ,pp. : 1050-1056

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A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration

By Ekström Ulf   Andréasson Sten   Ponjavic Vesna   Abrahamson Magnus   Sandgren Ola   Nilsson-Ehle Peter   Ehinger Berndt  

Ophthalmic Genetics, Vol. 19, Iss. 3, 1998-09 ,pp. : 149-156

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Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS

By Ekström Ulf   Ponjavic Vesna   Abrahamson Magnus   Nilsson-Ehle Peter   Andréasson Sten   Stenström Ingeborg   Ehinger Berndt  

Ophthalmic Genetics, Vol. 19, Iss. 1, 1998-03 ,pp. : 27-37

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