Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: Description of novel mutations and novel genotype–phenotype correlations-Reference-Cited by-同舟云学术

Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: Description of novel mutations and novel genotype–phenotype correlations

Published:2009-08 Issue:2 Volume:89 Page:172-177
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Zenteno Juan Carlos,Correa-Gomez Vicente,Santacruz-Valdez Concepción,Suarez-Sanchez Raul,Villanueva-Mendoza Cristina

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference27 articles.

1. Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene;Aldave;Am. J. Ophthalmol.,2004

2. Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene;Aldave;Mol. Vis.,2006

3. Elucidating the molecular genetic basis of the corneal dystrophies;Aldave;Arch. Ophthalmol.,2007

4. TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients;Chakravarthi;Invest. Ophthalmol. Vis. Sci.,2005

5. Corneal Dystrophies;Chang,1998

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1. Clinical and Histopathologic Characteristics and Template of the TGFBI p.(His626Arg) Missense Variant Lattice Corneal Dystrophy;Cornea;2023-02-10

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3. Maltese Allelic Variants in Corneal Dystrophy Genes in a Worldwide Setting;Molecular Diagnosis & Therapy;2022-07-07

4. Detailed phenotypic description of stromal corneal dystrophy in a large pedigree carrying the uncommon TGFBI p.Ala546Asp pathogenic variant;Ophthalmic Genetics;2022-04-26

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