MEDICAL SCIENCES Correction for “Mitochondrial Nuclear Retrograde Regulator 1 (MNRR1) rescues the cellular phenotype of MELAS by inducing homeostatic mechanisms,” by Siddhesh Aras, Neeraja Purandare, Stephanie Gladyck, Mallika Somayajulu-Nitu, Kezhong Zhang, Douglas C. Wallace, and Lawrence I. Grossman, which was first published November 30, 2020; 10.1073/pnas.2005877117 (Proc. Natl. Acad. Sci. U.S.A. 117, 32056–32065).
The authors note that an additional affiliation should be listed for Siddhesh Aras, Neeraja Purandare, and Lawrence I. Grossman. The new affiliation should appear as Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, US Department of Health and Human Services, Detroit, MI 48201. The corrected author and affiliation lines appear below. The online version has been corrected.
The authors also note that the following statement should be added to the Acknowledgments: “This work was also supported by the Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS); and, in part, with federal funds from NICHD/NIH/DHHS under Contract HHSN275201300006C.”
Siddhesh Arasa,b, Neeraja Purandarea,b, Stephanie Gladycka, Mallika Somayajulu-Nitua, Kezhong Zhanga, Douglas C. Wallacec,d, and Lawrence I. Grossmana,b
aCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201; bPerinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, US Department of Health and Human Services, Detroit, MI 48201; cCenter for Mitochondrial and Epigenomic Medicine, Children’s Hospital of Philadelphia Research Institute, Philadelphia, PA 19104; and dDepartment of Pediatrics, Division of Human Genetics, The Children’s Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104
