A case of familial hypertriglyceridemia associated with a novel heterozygous AGPAT2 mutation
The heterozygous AGPAT2 mutation may represent a novel genetic factor in familial hypertriglyceridemia. Further research is needed to clarify its clinical significance and inheritance mechanisms.
Authors
- Saleh Albanyan (ORCID: https://orcid.org/0000-0003-2839-8471)
- Turky H. Almigbal (ORCID: https://orcid.org/0000-0002-8029-3071)
- Ebtihal Y. Alyusuf (ORCID: https://orcid.org/0000-0002-9975-7622)
- Ibrahim Alsadhan (ORCID: https://orcid.org/0000-0003-4394-5146)
- Yazeed Alekrish (ORCID: https://orcid.org/0000-0001-5051-7700)
- Mohamed A. Al-Maatouq
- Nasser M. AbuDujain (ORCID: https://orcid.org/0000-0001-5290-1482)
- Aishah Ekhzaimy (ORCID: https://orcid.org/0000-0002-8024-0631)
Institutions
- Alfaisal University (SA)
- Salmaniya Medical Complex (BH)
- King Saud Medical City (SA)
- King Saud University (SA)
- King Khalid University Hospital (SA)
Publication Details
- Journal
- Annals of Medicine and Surgery
- Published
- 2025-03-18
- DOI
- https://doi.org/10.1097/ms9.0000000000003167
- Primary Topic
- Lipid metabolism and disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00