TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities
Authors:
- 1 December 2019
- journal article
- research article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 105 (6) , 1126-1147
Abstract
No abstract availableKeywords
Funding Information
- Rosetrees Trust
- National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology
- Brain Research UK
- Muscular Dystrophy UK
- Medical Research Council (MR/S01165X/1, G0601943, MR/S005021/1)
- Newlife – The Charity for Disabled Children
- European Cooperation in Science and Technology
- Wellcome Trust (WT104033AIA, WT093205)
- University College London
- ZonMw (91217045)
- Great Ormond Street Hospital Charity
- Multiple System Atrophy Trust
- Fonds Wetenschappelijk Onderzoek (V429317N)
- Fonds Wetenschappelijk Onderzoek
- Muscular Dystrophy Association (MDA USA)
- European Cooperation in Science and Technology (CA16118)
- Engineering Research Network Wales
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