Lenticulostriate vasculopathy in newborns: whole genome sequencing data analysis
The identification of this unique variant in <i>WNK1</i> provides a potential genetic link to the etiopathogenesis of LSV, offering new insights into this condition. However, further functional studies and more comprehensive genetic research are required to establish definitive associations.
Authors
- Vaidutis Kučinskas (ORCID: https://orcid.org/0000-0001-6433-7305)
- Yogen Singh (ORCID: https://orcid.org/0000-0002-5207-9019)
- Alina Urnikytė (ORCID: https://orcid.org/0000-0002-0764-0946)
- Svetlana Dauengauer‐Kirlienė (ORCID: https://orcid.org/0000-0003-3090-2526)
- Dovydas Pranauskas
Institutions
- Vilnius University (LT)
- Vilnius University of Applied Sciences (LT)
- UC Davis Children's Hospital (US)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2025-08-14
- DOI
- https://doi.org/10.3389/fped.2025.1531086
- Citations
- 1
- Primary Topic
- Congenital Heart Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.35