Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article.
- DOI
- 10.1097/md.0000000000000925
- Published
- 2015 Jun
- Container
- Medicine
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1097/md.0000000000000925,
title = {Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article.},
author = {Oussalah A and Bosco P and Anello G and Spada R and Guéant-Rodriguez RM and Chery C and Rouyer P and Josse T and Romano A and Elia M and Bronowicki JP and Guéant JL},
year = {2015},
journal = {Medicine},
doi = {10.1097/md.0000000000000925},
url = {https://doi.org/10.1097/md.0000000000000925}
}RIS
TY - JOUR TI - Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article. AU - Oussalah A AU - Bosco P AU - Anello G AU - Spada R AU - Guéant-Rodriguez RM AU - Chery C AU - Rouyer P AU - Josse T AU - Romano A AU - Elia M AU - Bronowicki JP AU - Guéant JL PY - 2015 JO - Medicine DO - 10.1097/md.0000000000000925 UR - https://doi.org/10.1097/md.0000000000000925 ER -
APA
A, O., P, B., G, A., R, S., RM, G., C, C., P, R., T, J., A, R., M, E., JP, B., & JL, G. (2015). Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article.. Medicine. https://doi.org/10.1097/md.0000000000000925
Source records
- pubmed · retrieved 2026-09-26T02:00:23.078Z