A Case of Familial Chylomicronemia Syndrome Caused by a Novel Homozygous GPIHBP1 Mutation Successfully Treated with the Selective PPARα Modulator Pemafibrate.
- DOI
- 10.5551/jat.66218
- Published
- 2026-06-17
- Container
- J Atheroscler Thromb
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.5551/jat.66218,
title = {A Case of Familial Chylomicronemia Syndrome Caused by a Novel Homozygous GPIHBP1 Mutation Successfully Treated with the Selective PPARα Modulator Pemafibrate.},
author = {Otsuki T and Chung Y and Kawachi Y and Komuku S and Yamanishi M and Takano T and Yamaguchi A and Hanada H and Masuda D and Miyashita K and Yamashita S.},
year = {2026},
journal = {J Atheroscler Thromb},
doi = {10.5551/jat.66218},
url = {https://doi.org/10.5551/jat.66218}
}RIS
TY - JOUR TI - A Case of Familial Chylomicronemia Syndrome Caused by a Novel Homozygous GPIHBP1 Mutation Successfully Treated with the Selective PPARα Modulator Pemafibrate. AU - Otsuki T AU - Chung Y AU - Kawachi Y AU - Komuku S AU - Yamanishi M AU - Takano T AU - Yamaguchi A AU - Hanada H AU - Masuda D AU - Miyashita K AU - Yamashita S. PY - 2026 JO - J Atheroscler Thromb DO - 10.5551/jat.66218 UR - https://doi.org/10.5551/jat.66218 ER -
APA
T, O., Y, C., Y, K., S, K., M, Y., T, T., A, Y., H, H., D, M., K, M., & S., Y. (2026). A Case of Familial Chylomicronemia Syndrome Caused by a Novel Homozygous GPIHBP1 Mutation Successfully Treated with the Selective PPARα Modulator Pemafibrate.. J Atheroscler Thromb. https://doi.org/10.5551/jat.66218
Source records
- europe-pmc · retrieved 2026-09-25T05:41:57.306Z