J. Luberichs

Extension of a recent therapy for dyslexia.

M. Fahle, J. Luberichs, 1995, German journal of ophthalmology.

Genetic animal models for retinal degeneration.

S. Fauser, F. Schüttauf, J. Luberichs, 2002, Survey of ophthalmology.

Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy

D. Besch, S. Fauser, B. Leo-Kottler, 2002, Ophthalmic genetics.

Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations.

D. Besch, S. Fauser, B. Leo-Kottler, 2002, Biochemical and biophysical research communications.

Leber’s hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery

D. Besch, S. Fauser, B. Leo-Kottler, 2002, Graefe’s Archive for Clinical and Experimental Ophthalmology.

A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy

D. Besch, S. Fauser, B. Leo-Kottler, 2002, Graefe's Archive for Clinical and Experimental Ophthalmology.