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ARVO Annual Meeting Abstract May 2006

A Yeast Two–Hybrid Screen for Clarin–1 (USH3A) Interacting Proteins

J. Isosomppi; A. Aittakorpi; H. Västinsalo; S.F. Geller; E.M. Sankila; J.G. Flannery

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2063.

ARVO Annual Meeting Abstract May 2005

Cellular Localization and Processing of USH3A Protein Clarin–1 in Transiently Transfected Cell Lines

J. Isosomppi; H. Västinsalo; S.F. Geller; J.G. Flannery; E.M. Sankila

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1641.

ARVO Annual Meeting Abstract May 2005

X–linked Cone–rod Dystrophy (CORDX3) Is Caused by Mutation in CACNA1F

R. Jalkanen; M. Mäntyjärvi; R. Tobias; J. Isosomppi; E.M. Sankila; T. Alitalo; N.T. Bech–Hansen

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1793.

ARVO Annual Meeting Abstract May 2004

Vision Loss in Usher Syndrome Type III is Caused by Mutations in Clarin–1, an Inner Retinal Protein.

S.F. Geller; J. Isosomppi; H. Makela; E.M. Sankila; P.T. Johnson; J.G. Flannery

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):5123.

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