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ARVO Annual Meeting Abstract April 2011

Autofluorescence Study In NR2E3 p.G56R-linked Autosomal Dominant Retinitis Pigmentosa In A Single Kindred

Hoai V. Tran; Pascal Escher; Veronika Vaclavik; Isabelle Favre; Hasret Bajrami; Francois X. Borruat; Daniel F. Schorderet; Francis L. Munier

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):6604.

ARVO Annual Meeting Abstract April 2011

Phenotype of two Consanguineous Autosomic Recessive Retinitis Pigmentosa Families Caused by PDE6A and PDE6B Mutations

Leila Largueche; Karim Baklouti; Ahlem Merdassi; Ibtissem Chouchane; Mejda Bouladi; Isabelle Favre; Hasret Bajrami; Daniel F. Schorderet; Francis L. Munier; Leila El Matri

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):2372.

ARVO Annual Meeting Abstract April 2011

A Novel Homozygous R764H Mutation in CRB1 Causes Autosomal Recessive Retinitis Pigmentosa in a Consanguineous Family

Leila Bouayed-Tiab; Leila Largueche; Ibtissem Chouchane; Kaouthar Derouiche; Hasret Bajrami; Isabelle Favre; Francis L. Munier; Leila El Matri; Daniel F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):2374.

ARVO Annual Meeting Abstract April 2011

Phenotype in Two Consanguineous Tunisian Families With non Syndromic Autosomic Recessive Retinitis Pigmentosa Caused by an USH2A Mutation

Ahmed Chebil; Leila Largueche; Fedra Kort; Rim Bouraoui; Kaouther Derouiche; Isabelle Favre; Hasret Bajrami; Francis L. Munier; Daniel F. Schorderet; Leila El Matri

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):2395.

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