Heimer, Gali
Kerätär, Juha M.
Riley, Lisa G.
Balasubramaniam, Shanti
Eyal, Eran
Pietikäinen, Laura P.
Hiltunen, J. Kalervo
Marek-Yagel, Dina
Hamada, Jeffrey
Gregory, Allison
Rogers, Caleb
Hogarth, Penelope
Nance, Martha A.
Shalva, Nechama
Veber, Alvit
Tzadok, Michal
Nissenkorn, Andreea
Tonduti, Davide
Renaldo, Florence
Kraoua, Ichraf
Panteghini, Celeste
Valletta, Lorella
Garavaglia, Barbara
Cowley, Mark J.
Gayevskiy, Velimir
Roscioli, Tony
Silberstein, Jonathon M.
Hoffmann, Chen
Raas-Rothschild, Annick
Tiranti, Valeria
Anikster, Yair
Christodoulou, John
Kastaniotis, Alexander J.
Ben-Zeev, Bruria
Hayflick, Susan J.
Bamshad, Michael J.
Leal, Suzanne M.
Nickerson, Deborah A.
Anderson, Peter
Annable, Marcus
Blue, Elizabeth Marchani
Buckingham, Kati J.
Chin, Jennifer
Chong, Jessica X.
Cornejo, Rodolfo Jr.
Davis, Colleen P.
Frazar, Christopher
He, Zongxiao
Jarvik, Gail P.
Jimenez, Guillaume
Johanson, Eric
Kolar, Tom
Krauter, Stephanie A.
Luksic, Daniel
Marvin, Colby T.
McGee, Sean
McGoldrick, Daniel J.
Patterson, Karynne
Perez, Marcos
Phillips, Sam W.
Pijoan, Jessica
Robertson, Peggy D.
Santos-Cortez, Regie
Shankar, Aditi
Slattery, Krystal
Shively, Kathryn M.
Siegel, Deborah L.
Smith, Joshua D.
Tackett, Monica
Wang, Gao
Wegener, Marc
Weiss, Jeffrey M.
Wernick, Riana I.
Wheeler, Marsha M.
Yi, Qian
Funding for this research was provided by:
Israel Science Foundation (2023/14)
Pinchas Borenstein Talpiot Medical Leadership Program
Sigrid Juselius Foundation
Academy of Finland
NBIA Disorders Association
National Human Genome Research Institute
National Heart, Lung and Blood Institute (2UM1HG006493)
New South Wales Office of Health and Medical Research Council Sydney Genomics
NHMRC (1026891)
Cancer Institute NSW (13/ECF/1-46)
Kinghorn Foundation
Crane
Perkins families
Pierfranco and Luisa Mariani Foundation
TELETHON Italy (GTB09003)
This article is maintained by: Elsevier
Article Title: MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2016.09.021
Content Type: article
Copyright: © 2016 American Society of Human Genetics.