A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease
- DOI
- 10.1016/s0021-9150(00)81416-1
- Published
- 2000-07
- Container
- Atherosclerosis
- Publisher
- Elsevier BV
- Open access
- unknown
Credibility signals
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Cite this work
BibTeX
@article{allodium:10.1016/s0021-9150-00-81416-1,
title = {A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease},
author = {S. Bertolini and L. Pisciotta and M. Seri and R. Cusano and A. Cantafora and L. Calabresi and G. Franceschini and R. Ravazzolo and S. Calandra},
year = {2000},
journal = {Atherosclerosis},
doi = {10.1016/s0021-9150(00)81416-1},
url = {https://doi.org/10.1016/s0021-9150(00)81416-1}
}RIS
TY - JOUR TI - A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease AU - S. Bertolini AU - L. Pisciotta AU - M. Seri AU - R. Cusano AU - A. Cantafora AU - L. Calabresi AU - G. Franceschini AU - R. Ravazzolo AU - S. Calandra PY - 2000 JO - Atherosclerosis DO - 10.1016/s0021-9150(00)81416-1 UR - https://doi.org/10.1016/s0021-9150(00)81416-1 ER -
APA
Bertolini, S., Pisciotta, L., Seri, M., Cusano, R., Cantafora, A., Calabresi, L., Franceschini, G., Ravazzolo, R., & Calandra, S. (2000). A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease. Atherosclerosis. https://doi.org/10.1016/s0021-9150(00)81416-1
Source records
- crossref · retrieved 2026-09-26T10:19:52.774Z