Clinical and Structural Characterization of a Novel TGFBI Mutation Linked to a Lattice Corneal Dystrophy Variant in a Greek Family.

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Bibliographic Details
Title: Clinical and Structural Characterization of a Novel TGFBI Mutation Linked to a Lattice Corneal Dystrophy Variant in a Greek Family.
Authors: Zacharogianni M; From the Independent Author (M.Z.)., Papandreou NC; Department of Biology, School of Sciences (N.C.P.), Section of Cell Biology and Biophysics, National and Kapodistrian University of Athens, Athens, Greece., Marinakis NM; Laboratory of Medical Genetics (N.M.M., F.N.T., and J.T.S.), St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece; Research University Institute for the Study and Prevention of Genetic and Malignant Disease of Childhood (N.M.M.), St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece., Tilemis FN; Laboratory of Medical Genetics (N.M.M., F.N.T., and J.T.S.), St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece., Traeger-Synodinos J; Laboratory of Medical Genetics (N.M.M., F.N.T., and J.T.S.), St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece., Palioura S; Department of Ophthalmology (S.P.), University of Cyprus Medical School, Nicosia, Cyprus. Electronic address: sotiria.palioura@gmail.com.
Source: American journal of ophthalmology [Am J Ophthalmol] 2025 Jun; Vol. 274, pp. 112-121. Date of Electronic Publication: 2025 Mar 04.
Publication Type: Journal Article
Journal Info: Publisher: Elsevier Science Country of Publication: United States NLM ID: 0370500 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-1891 (Electronic) Linking ISSN: 00029394 NLM ISO Abbreviation: Am J Ophthalmol Subsets: MEDLINE
Database: MEDLINE Ultimate
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