Late-onset lattice corneal dystrophy associated TGFBI p.H626R mutation in members of a Canadian family

Author:

Chao-Shern Connie,DeDionisio Larry A.,Chan Clara C.,Nesbit M. Andrew,McMullen C.B. Tara

Publisher

Elsevier BV

Subject

Ophthalmology,General Medicine

Reference13 articles.

1. Structural and functional implications of human transforming growth factor β-induced protein, TGFBIp, in corneal dystrophies;García-Castellanos;Structure,2017

2. Trauma-induced exacerbation of epithelial-stromal TGFBI lattice corneal dystrophy;Nithianandan;Can J Ophthalmol,2019

3. Genotype-phenotype correlation for TGFBI corneal dystrophies identifies p.(G623D) as a novel cause of epithelial basement membrane dystrophy;Evans;Invest Ophthalmol Vis Sci,2016

4. Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature;Yang;Mol Vis,2010

5. Genetic and phenotypic investigation of a Chinese pedigree with lattice corneal dystrophy IIIB subtype;Wang;Eye Sci,2013

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