N Tijmes

Retinal arterial changes correlate with cerebral small-vessel disease

J. Stam, J Stam, V. Kwa, 2002, Neurology.

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.

K Rohrschneider, A Blankenagel, B. J. Klevering, 1999, American journal of human genetics.

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.

K Rohrschneider, A Blankenagel, A. Deutman, 1998, Human molecular genetics.