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ARVO Annual Meeting Abstract May 2006

A Novel CACNA1F Gene Mutation in the Original Family With Åland Island Eye Disease

R. Jalkanen; N.T. Bech–Hansen; R. Tobias; A. de la Chapelle; H. Forsius; T. Alitalo

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4625.

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

Mutation of the Calcium Channel Gene Cacna1f Disrupts Calcium Signaling and Synaptic Transmission in Mouse Retina

N.C. Orton; F.C. Mansergh; J.P. Vessey; M. Lalonde; F. Tremblay; S. Barnes; D.E. Rancourt; W.K. Stell; N.T. Bech–Hansen

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2507.

ARVO Annual Meeting Abstract May 2003

Characterization of the Genotype and Phenotype of Congenital Stationary Night Blindness in Atlantic Canada

B.A. Ford; J. Beis; F. Tremblay; I. DeBecker; N.T. Bech-Hansen; J. Robitaille

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):1479.

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