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ARVO Annual Meeting Abstract May 2008

Mutation Spectrum of Usher Syndrome in Finland

H. Vastinsalo; J. Isosomppi; L. Kleemola; L. Jauhola; E.-M. Sankila

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):2121. doi:

ARVO Annual Meeting Abstract May 2007

Alternative Splice Variants of the Usher Syndrome Type 3 (USH3) Gene Clarin 1 (CLRN1)

H. Vastinsalo; J. Isosomppi; A. Dinculescu; W. W. Hauswirth; S. Geller; J. Flannery; E.-M. Sankila

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):3791. doi:

ARVO Annual Meeting Abstract May 2006

Functional Evaluation of Two Novel Ush3a Mutations by in vitro Expression

H.M. Vastinsalo; J. Isosomppi; S. Geller; J. Flannery; E. Heon; E.–M. Sankila

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2062. doi:

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. doi:

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. doi:

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. doi:

ARVO Annual Meeting Abstract May 2005

Two Novel Mutations in Myosin VIIA Cause USH1B in a Compound Heterozygote Finnish Patient

H.M. Vastinsalo; J. Isosomppi; E.–M. Sankila

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1800. doi:

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. doi:

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