The rs10191329 Risk Allele is Associated with Retinal Layer Thinning in Multiple Sclerosis (P6-1.013)
To investigate whether the rs10191329 variant is associated with retinal layer thinning in relapsing multiple sclerosis (MS).
Authors
- Harald Hegen
- Gabriel Bsteh (ORCID: https://orcid.org/0000-0002-0825-0851)
- Berthold Pemp (ORCID: https://orcid.org/0000-0002-0569-0229)
- Markus Ponleitner (ORCID: https://orcid.org/0000-0002-3709-1845)
- Nik Krajnc (ORCID: https://orcid.org/0000-0002-4146-5870)
- Martin Krenn (ORCID: https://orcid.org/0000-0003-3026-3082)
- Thomas Berger (ORCID: https://orcid.org/0000-0002-2062-5193)
- Theresa König (ORCID: https://orcid.org/0000-0002-7904-8482)
- Fabian Föttinger (ORCID: https://orcid.org/0009-0005-7970-5349)
Institutions
- Innsbruck Medical University (AT)
- Universität Innsbruck (AT)
- Neurology, Inc (US)
- Medical University of Vienna (AT)
Publication Details
- Journal
- Neurology
- Published
- 2025-04-07
- DOI
- https://doi.org/10.1212/wnl.0000000000211122
- Primary Topic
- Genomic variations and chromosomal abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00