De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies
Open Access
- 8 August 2019
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 105 (3), 640-657
- https://doi.org/10.1016/j.ajhg.2019.07.005
Abstract
No abstract availableFunding Information
- Baillie Gifford
- Visually Impaired Children Taking Action
- Microphthalmia, Anophthalmia and Coloboma Support
- HEIF
- La Fondation De France (2015-00060235)
- Fondation Maladies Rares and Retina France
- Fondazione Bambino Gesù
- E-Rare
- AIRC (IG 21614)
- Italian Ministry of Health
- National Heart, Lung, and Blood Institute (R35 HL135742)
- French National Research Agency (ANR-10-COHO-0003)
- UCB Celltech
- Duke Genome Sequencing Clinic
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (R01NS058721)
- MRC (MR/L003775/1)
- Wellcome Trust (104682/Z/14/Z)
- Joint MRC/Wellcome Trust (MR/R006237/1)
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