Case Report: A heterozygous loss-of-function variant of the ERG gene in a family with vascular pathologies
Our report discusses the possibility that loss-of-function variants in <i>ERG</i> may act as a risk factor for arterial disease.
Authors
- Dittmar Böckler (ORCID: https://orcid.org/0000-0003-2421-2019)
- Christian Patrick Schaaf (ORCID: https://orcid.org/0000-0002-2148-7490)
- Nicola Dikow (ORCID: https://orcid.org/0000-0003-4631-9829)
- Philipp Erhart (ORCID: https://orcid.org/0000-0002-4964-2448)
- Hamish S. Scott (ORCID: https://orcid.org/0000-0002-5813-631X)
- Susanne Dihlmann (ORCID: https://orcid.org/0000-0002-3737-7755)
- Caspar Grond‐Ginsbach
- Daniel Körfer (ORCID: https://orcid.org/0000-0002-8242-2076)
- Christopher N Hahn (ORCID: https://orcid.org/0000-0001-5105-2554)
- Felix Marbach (ORCID: https://orcid.org/0000-0003-3953-6235)
- Eva Maria Christina Schwaibold (ORCID: https://orcid.org/0000-0003-2708-9642)
- Sabrina Oeser (ORCID: https://orcid.org/0009-0007-1915-5415)
- Katrin Hinderhofer (ORCID: https://orcid.org/0000-0003-1493-4608)
- Jiarna R. Zerella
Institutions
- University of Bonn (DE)
- Heidelberg University (DE)
- University Hospital Heidelberg (DE)
- Centre for Cancer Biology (AU)
- The University of Adelaide (AU)
Publication Details
- Journal
- Frontiers in Cardiovascular Medicine
- Published
- 2025-06-24
- DOI
- https://doi.org/10.3389/fcvm.2025.1550523
- Primary Topic
- Cerebrovascular and genetic disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Heidelberger Stiftung Chirurgie