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Authors
Pinard, Amélie https://orcid.org/0000-0003-1882-5740
Guey, Stéphanie
Guo, Dongchuan
Cecchi, Alana C.
Kharas, Natasha
Wallace, Stephanie
Regalado, Ellen S.
Hostetler, Ellen M. https://orcid.org/0000-0002-9258-7827
Sharrief, Anjail Z.
Bergametti, Françoise
Kossorotoff, Manoelle https://orcid.org/0000-0002-0813-9045
Hervé, Dominique https://orcid.org/0000-0001-6197-6275
Kraemer, Markus https://orcid.org/0000-0002-5667-3621
Bamshad, Michael J.
Nickerson, Deborah A.
Smith, Edward R.
Tournier-Lasserve, Elisabeth
Milewicz, Dianna M.
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Funding
Funding for this research was provided by:
American Heart Association (18POST34020031)
Fibromuscular Dysplasia Project
Fondation pour la Recherche Médicale
Henrietta B. and Frederik H. Bugher Foundation
INSERM
National Human Genome Research Institute and the National Heart, Lung and Blood Institute (HG006493)
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More Information
This article is maintained by: Elsevier
Article Title: The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0639-2
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
