F J van Haren

The organization of the reciprocal connections between the subiculum and the entorhinal cortex in the cat: I. A neuroanatomical tracing study

M P Witter, M. Witter, H. Groenewegen, 1986, The Journal of comparative 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.