Genetic Analysis of a Rare Patient Case with Complex Autoimmune, Neurological, Blood, and Heart Disease Comorbidities.
This study analyzes a rare patient with SLE, AAG, TTP, and LVNC using whole genome sequencing. It identifies common and rare genetic mutations linked to these diseases. The work highlights the value of patient-partnered genomics in understanding complex comorbidities.
Authors
- Yuelin Shen (ORCID: https://orcid.org/0009-0007-3206-610X)
- Zhinan Lin (ORCID: https://orcid.org/0009-0007-5416-6961)
- Pauline A. Kane
- Xiaohua Zhu
- Christine Von Raesfeld (ORCID: https://orcid.org/0009-0000-6767-3160)
- Jaime Raijman
Institutions
- Maxygen (United States) (US)
- City University of Hong Kong (HK)
- Palo Alto University (US)
- San Francisco Foundation (US)
Publication Details
- Published
- 2025-05-05
- DOI
- https://doi.org/10.21428/a2fa6306.98b1af9a
- Primary Topic
- Diabetes and associated disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- City University of Hong Kong