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Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder

Christos Chinopoulos, Spyros Batzios, Lambertus P. van den Heuvel, Richard J. Rodenburg, Roel Smeets, Hans R. Waterham, Marjolein Turkenburg, Jos P.N. Ruiter, Ronald J. A. Wanders, Judit Dóczi,

Molecular Genetics and Metabolism · 2018 · 34 citations · 25 references

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25

Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion

Orly Elpeleg, Chaya Miller, Eli Hershkovitz et al. · The American Journal of Human Genetics · 2005 · 313 citations · Full text

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Mitochondrial disorders

Nicole I. Wolf · Neurology · 2002 · 231 citations

, , +17

SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness

Rosalba Carrozzo, Carlo Dionisi‐Vici, Ulrike Steuerwald et al. · Brain · 2007 · 207 citations · Full text

, , +17

Deficiency of the α Subunit of Succinate–Coenzyme A Ligase Causes Fatal Infantile Lactic Acidosis with Mitochondrial DNA Depletion

Elsebet Østergaard, Ernst Christensen, Elisabeth Kristensen et al. · The American Journal of Human Genetics · 2007 · 182 citations · Full text

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Genetic Evidence for the Expression of ATP- and GTP-specific Succinyl-CoA Synthetases in Multicellular Eucaryotes

James D. Johnson, James G. Mehus, K Tews et al. · Journal of Biological Chemistry · 1998 · 160 citations · Full text

, , +12