A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann’s corneal dystrophy

Authors

Lori S. Sullivan, University of Texas Health Science Center at Houston
Eric B. Baylin, University of Texas Health Science Center at Houston
Ramon Font, Baylor College of Medicine
Stephen P. Daiger, University of Texas Health Science Center at Houston
Jay S. Pepose, Washington University School of Medicine in St. Louis
Thomas E. Clinch, University of Utah
Hisashi Nakamura, University of Texas Health Science Center at Houston
Xinping C. Zhao, University of Texas Health Science Center at Houston
Richard W. Yee, University of Texas Health Science Center at Houston

Journal

Molecular Vision

Publication Date

2007

Volume

13

Inclusive Pages

975-980

Document Type

Open Access Publication

Rights and Permissions

Sullivan, L. S., Baylin, E. B., Font, R., Daiger, S. P., Pepose, J. S., Clinch, T. E., . . . Yee, R. W. (2007). A novel mutation of the keratin 12 gene responsible for a severe phenotype of meesmann's corneal dystrophy. Molecular Vision, 13, 975-980. http://www.molvis.org/molvis/v13/a103/

Recommended Citation

Sullivan, Lori S.; Baylin, Eric B.; Font, Ramon; Daiger, Stephen P.; Pepose, Jay S.; Clinch, Thomas E.; Nakamura, Hisashi; Zhao, Xinping C.; and Yee, Richard W., "A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann’s corneal dystrophy." Molecular Vision. 13, 975-980. (2007).
https://digitalcommons.wustl.edu/open_access_pubs/1809