A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemia

Michael M Page; Katrina L Ellis; Dick C Chan; Jing Pang; Amanda J Hooper; Damon A Bell; John R Burnett; Eric K Moses; Gerald F Watts

doi:10.1016/j.jacl.2022.05.065

A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemia

Michael M Page, Katrina L Ellis, Dick C Chan, Jing Pang, Amanda J Hooper, Damon A Bell, John R Burnett, Eric K Moses, Gerald F Watts

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

Original language	English
Pages (from-to)	525-529
Number of pages	5
Journal	Journal of Clinical Lipidology
Volume	16
Issue number	4
DOIs	https://doi.org/10.1016/j.jacl.2022.05.065
Publication status	Published - 1 Jul 2022

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Page, M. M., Ellis, K. L., Chan, D. C., Pang, J., Hooper, A. J., Bell, D. A., Burnett, J. R., Moses, E. K., & Watts, G. F. (2022). A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemia. Journal of Clinical Lipidology, 16(4), 525-529. https://doi.org/10.1016/j.jacl.2022.05.065

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author = "Page, {Michael M} and Ellis, {Katrina L} and Chan, {Dick C} and Jing Pang and Hooper, {Amanda J} and Bell, {Damon A} and Burnett, {John R} and Moses, {Eric K} and Watts, {Gerald F}",

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AU - Pang, Jing

AU - Hooper, Amanda J

AU - Bell, Damon A

AU - Burnett, John R

AU - Moses, Eric K

AU - Watts, Gerald F

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A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemia

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