Extreme HDL-C elevation associated with homozygous CETP deficiency and a SCARB1 variant: A case illustrating the HDL paradox

Serpil Dinç, Levent Özsarı, Fatih Yeşildal, Hamdi Kale, Adnan Gökçel

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DOI
10.1016/j.jacl.2026.10.007
Published
2026-10
Container
Journal of Clinical Lipidology
Publisher
Elsevier BV
Open access
unknown

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BibTeX

@article{allodium:10.1016/j.jacl.2026.10.007,
  title = {Extreme HDL-C elevation associated with homozygous CETP deficiency and a SCARB1 variant: A case illustrating the HDL paradox},
  author = {Serpil Dinç and Levent Özsarı and Fatih Yeşildal and Hamdi Kale and Adnan Gökçel},
  year = {2026},
  journal = {Journal of Clinical Lipidology},
  doi = {10.1016/j.jacl.2026.10.007},
  url = {https://doi.org/10.1016/j.jacl.2026.10.007}
}

RIS

TY  - JOUR
TI  - Extreme HDL-C elevation associated with homozygous CETP deficiency and a SCARB1 variant: A case illustrating the HDL paradox
AU  - Serpil Dinç
AU  - Levent Özsarı
AU  - Fatih Yeşildal
AU  - Hamdi Kale
AU  - Adnan Gökçel
PY  - 2026
JO  - Journal of Clinical Lipidology
DO  - 10.1016/j.jacl.2026.10.007
UR  - https://doi.org/10.1016/j.jacl.2026.10.007
ER  - 

APA

Dinç, S., Özsarı, L., Yeşildal, F., Kale, H., & Gökçel, A. (2026). Extreme HDL-C elevation associated with homozygous CETP deficiency and a SCARB1 variant: A case illustrating the HDL paradox. Journal of Clinical Lipidology. https://doi.org/10.1016/j.jacl.2026.10.007

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