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Paper Details

Confirmation of association of <i>TGFBI</i> p.Ser591Phe mutation with variant lattice corneal dystrophy.
Ophthalmic Genet
0
2022
Author NameAffiliation
Jens MeilerCenter for Structural Biology, Vanderbilt University
Jens MeilerVanderbilt University
Jens MeilerInstitute of Drug Discovery, University of Leipzig
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Release 1.2