Genomic Landscape of Chromosome X Factor VIII: From Hemophilia A in Males to Risk Variants in Females
This work highlights the need to define missense variants, especially those for VUS and from subjects of non-European ancestry, as well as the roles of these variants in women's physiology.
Authors
- Disha Bhargava
- Shawn M. Jobe (ORCID: https://orcid.org/0000-0001-7878-6101)
- Michèle Morris (ORCID: https://orcid.org/0000-0003-2529-4597)
- Jena M. Krueger (ORCID: https://orcid.org/0009-0009-3471-3395)
- Olivia Morris (ORCID: https://orcid.org/0000-0002-9491-8060)
- Cynthia L. Stenger (ORCID: https://orcid.org/0000-0001-7014-4243)
- Jeremy W. Prokop (ORCID: https://orcid.org/0000-0002-1818-9695)
- Sanjana Arora
Institutions
- University of North Alabama (US)
- Helen DeVos Children's Hospital (US)
- HudsonAlpha Institute for Biotechnology (US)
- Corewell Health
- Michigan State University (US)
Publication Details
- Journal
- Genes
- Published
- 2024-11-27
- DOI
- https://doi.org/10.3390/genes15121522
- Citations
- 1
- Primary Topic
- Cancer-related gene regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.23
Funders
- National Science Foundation
- American Heart Association
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases