Keshavan, Nandaki http://orcid.org/0000-0001-6939-4528
Abdenur, Jose http://orcid.org/0000-0002-4671-1241
Anderson, Glenn
Assouline, Zahra
Barcia, Giulia
Bouhikbar, Lamia
Chakrapani, Anupam http://orcid.org/0000-0003-3745-0550
Cleary, Maureen
Cohen, Marta C. http://orcid.org/0000-0001-5534-444X
Feillet, François http://orcid.org/0000-0002-6814-0806
Fratter, Carl http://orcid.org/0000-0001-7125-5391
Hauser, Natalie http://orcid.org/0000-0001-7663-1851
Jacques, Tom
Lam, Amanda
McCullagh, Helen
Phadke, Rahul http://orcid.org/0000-0001-9699-2718
Rötig, Agnès
Sharrard, Mark
Simon, Mariella http://orcid.org/0000-0002-8200-3277
Smith, Conrad
Sommerville, Ewen W.
Taylor, Robert W. http://orcid.org/0000-0002-7768-8873
Yue, Wyatt W.
Rahman, Shamima http://orcid.org/0000-0003-2088-730X
Funding for this research was provided by:
Great Ormond Street Hospital Children's Charity (V1260)
Wellcome Centre for Mitochondrial Research (203105/Z/16/Z)
Medical Research Council (MRC) Centre for Translational Research in Neuromuscular Disease (G0800674)
This article is maintained by: Elsevier
Article Title: The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0613-z
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics