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Funding for this research was provided by:
National Institutes of Health (R24OD026591, U01HG00794)
Cullen Foundation
This article is maintained by: Elsevier
Article Title: Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01216-8
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics