A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases.
- DOI
- 10.1016/j.atherosclerosis.2021.02.020
- Published
- 2021 Apr
- Container
- Atherosclerosis
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.atherosclerosis.2021.02.020,
title = {A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases.},
author = {Lima JG and Helena C Nobrega L and Moura Bandeira FT and Pires Sousa AG and Medeiros de Araujo Macedo TB and Cavalcante Nogueira AC and Fernandes de Oliveira Filho A and Alves RJ and Costa Gurgel Castelo MH and Silva Coelho FM and Maia RE and Lima DN and Timoteo ARS and de Melo Campos JTA},
year = {2021},
journal = {Atherosclerosis},
doi = {10.1016/j.atherosclerosis.2021.02.020},
url = {https://doi.org/10.1016/j.atherosclerosis.2021.02.020}
}RIS
TY - JOUR TI - A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases. AU - Lima JG AU - Helena C Nobrega L AU - Moura Bandeira FT AU - Pires Sousa AG AU - Medeiros de Araujo Macedo TB AU - Cavalcante Nogueira AC AU - Fernandes de Oliveira Filho A AU - Alves RJ AU - Costa Gurgel Castelo MH AU - Silva Coelho FM AU - Maia RE AU - Lima DN AU - Timoteo ARS AU - de Melo Campos JTA PY - 2021 JO - Atherosclerosis DO - 10.1016/j.atherosclerosis.2021.02.020 UR - https://doi.org/10.1016/j.atherosclerosis.2021.02.020 ER -
APA
JG, L., L, H. C. N., FT, M. B., AG, P. S., TB, M. D. A. M., AC, C. N., A, F. D. O. F., RJ, A., MH, C. G. C., FM, S. C., RE, M., DN, L., ARS, T., & JTA, D. M. C. (2021). A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases.. Atherosclerosis. https://doi.org/10.1016/j.atherosclerosis.2021.02.020
Source records
- pubmed · retrieved 2026-09-26T18:50:19.808Z