R. Bezold

Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.

K. Gerbitz, S. Hofmann, W. Rabl, 1997, Genomics.

Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease.

K. Gerbitz, S. Hofmann, M. Jaksch, 1997, Human molecular genetics.

DIDMOAD or Wolfram Syndrome: A mitochondrial-mediated disorder?

K. Gerbitz, S. Hofmann, M. Jaksch, 1995, Diabetes Care.

Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndrome

K. Gerbitz, S. Hofmann, M. Jaksch, 1997, Molecular and Cellular Biochemistry.

Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations.

K. Gerbitz, S. Hofmann, M. Jaksch, 1997, American journal of human genetics.