Concepedia

Correlation between clinical and molecular features in two MELAS families

Andrea Martinuzzi, Luigi Bartolomei, Rosalba Carrozzo, M.L. Mostacciuolo, Costantino Carbonin, Vito Toso, Emma Ciafaloni, Sara Shanske, S. DiMauro, C. Angelini

Journal of the Neurological Sciences · 1992 · 45 citations · 21 references

DOI

Concepts

References

21

Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy

Douglas C. Wallace, Gurparkash Singh, Marie T. Lott et al. · Science · 1988 · 2.4K citations

, , +17

A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

Yu‐ichi Goto, Ikuya Nonaka, Satoshi Horai · Nature · 1990 · 2.1K citations

, , +11

Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by Complementation

Michael P. King, Giuseppe Attardi · Science · 1989 · 1.6K citations

, , +14

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation

John M. Shoffner, Marie T. Lott, Angela Maria Serena Lezza et al. · Cell · 1990 · 1.5K citations

, , +16

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

Trends in Genetics · 1990 · 1.4K citations

, , +14