RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability
Open Access
- 30 March 2020
- journal article
- letter
- Published by Oxford University Press (OUP) in Brain
- Vol. 143 (4), e31
- https://doi.org/10.1093/brain/awaa070
Abstract
No abstract availableFunding Information
- University of Maryland
- National Institute of Neurological Disorders and Stroke
- NINDS (R01NS107428)
- Medical Research Council
- MRC (MR/S01165X/1, MR/S005021/1, G0601943)
- the National Institute for Health Research University College London Hospitals Biomedical Research Centre
- Multiple System Atrophy Trust
- Brain Research UK
- Sparks Great Ormond Street Hospital Charity, Muscular Dystrophy
- Muscular Dystrophy Association
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