SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19743-4

By:

• Gut, Philipp;
• Matilainen, Sanna;
• Meyer, Jesse G.;
• Pällijeff, Pieti;
• Richard, Joy;
• Carroll, Christopher J.;
• Euro, Liliya;
• Jackson, Christopher B.;
• Isohanni, Pirjo;
• Minassian, Berge A.;
• Alkhater, Reem A.;
• Østergaard, Elsebet;
• Civiletto, Gabriele;
• Parisi, Alice;
• Thevenet, Jonathan;
• Rardin, Matthew J.;
• He, Wenjuan;
• Nishida, Yuya;
• Newman, John C.;
• Liu, Xiaojing

Publication type:

Article