Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus. Mol Vis. 2011 Feb 15; 17:481-5.

View in: PubMed

Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.