APA (7th ed.) Citation

B, A., D, A., S, S., W, L., U, H., S, A., . . . M, A. (2025). Targeted sequencing with single-molecule molecular inversion probes highlights a gap in understanding the cause of Fuchs endothelial corneal dystrophy. Molecular vision, 31, 486.

Chicago Style (17th ed.) Citation

B, Alayed, Albuainain D, Siddiqui S, Li W, Hany U, Anand S, Inglehearn CF, Watson CM, and Ali M. "Targeted Sequencing with Single-molecule Molecular Inversion Probes Highlights a Gap in Understanding the Cause of Fuchs Endothelial Corneal Dystrophy." Molecular Vision 31 (2025): 486.

MLA (9th ed.) Citation

B, Alayed, et al. "Targeted Sequencing with Single-molecule Molecular Inversion Probes Highlights a Gap in Understanding the Cause of Fuchs Endothelial Corneal Dystrophy." Molecular Vision, vol. 31, 2025, p. 486.