Yu, Y., Triebwasser, M. P., Wong, E. K. S., Schramm, E. C., Thomas, B., Reynolds, R., . . . Seddon, J. M. (2014). Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration. Oxford University Press.
Stile di citazione ChicagoYu, Yi, et al. Whole-exome Sequencing Identifies Rare, Functional CFH Variants in Families With Macular Degeneration. Oxford University Press, 2014.
Citazione MLAYu, Yi, et al. Whole-exome Sequencing Identifies Rare, Functional CFH Variants in Families With Macular Degeneration. Oxford University Press, 2014.
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