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Published in 2022 at "Ophthalmic Genetics"
DOI: 10.1080/13816810.2022.2050766
Abstract: ABSTRACT Purpose To provide the initial confirmation of the c.1772C>T (p.Ser591Phe) mutation in the transforming growth factor- -induced (TGFBI) gene as being associated with variant lattice corneal dystrophy (LCD). Methods Ophthalmologic examination of the proband…
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Keywords:
ser591phe mutation;
variant lattice;
lattice corneal;
mutation ... See more keywords