Alexander S. Voljavec

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

John M. Shoffner, Marie T. Lott, Alexander S. Voljavec et al. · Proceedings of the National Academy of Sciences · 1989 · 507 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

M.D. Brown, Alexander S. Voljavec, Marie T. Lott et al. · Genetics · 1992 · 277 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Variable Genotype of Leber's Hereditary Optic Neuropathy Patients

Marie T. Lott, Alexander S. Voljavec, Douglas C. Wallace · American Journal of Ophthalmology · 1990 · 112 citations

Life Sciences, Genetics, Molecular Genetics +13

Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV

Xianxian Zheng, J. M. Shoffner, Marie T. Lott et al. · Neurology · 1989 · 77 citations

Life Sciences, Genetics, Molecular Genetics +17

Mitochondrial DNA Mutations Associated with Neuromuscular Diseases: Analysis and Diagnosis Using the Polymerase Chain Reaction

Douglas C. Wallace, Marie T. Lott, Angela Maria Serena Lezza et al. · Pediatric Research · 1990 · 24 citations

Medicine, Genetics, Molecular Genetics +17