Transforming growth factor beta‐induced p.(L558P) variant is associated with autosomal dominant lattice corneal dystrophy type IV in a large cohort of Spanish patients-Reference-Cited by-同舟云学术

Transforming growth factor beta‐induced p.(L558P) variant is associated with autosomal dominant lattice corneal dystrophy type IV in a large cohort of Spanish patients

Published:2019-05-22 Issue:7 Volume:47 Page:871-880
ISSN:1442-6404
Container-title:Clinical & Experimental Ophthalmology
language:en
Short-container-title:Clin Experiment Ophthalmol

Author:

Campos‐Mollo Ezequiel¹²,Varela‐Conde Yago³^ORCID,Arriola‐Villalobos Pedro²⁴⁵,Cabrera‐Beyrouti Rubén⁶,Benítez‐del‐Castillo José‐Manuel²⁴⁵⁷⁸,Maldonado Miguel J.²⁹^ORCID,Escribano Julio²¹⁰^ORCID

Affiliation:

1. Ophthalmology DepartmentHospital Virgen de los Lirios Alcoy Spain

2. Cooperative Research Network on Age‐Related Ocular Pathology, Visual and Life QualityInstitute of Health Carlos III Madrid Spain

3. Ophthalmology DepartmentHospital Universitario Río Hortega Valladolid Spain

4. Ophthalmology DepartmentHospital Clínico San Carlos Madrid Spain

5. Institute of Health ResearchHospital Clínico San Carlos Madrid Spain

6. Ophthalmology DepartmentHospital de Lluís Alcanyís Alicante Spain

7. Immunology, Ophthalmology and Otorhinolaryngology DepartmentComplutense University Madrid Spain

8. Rementería Clinic Madrid Spain

9. Institute of Applied Ophthalmobiology (IOBA‐Eye Institute)University of Valladolid Valladolid Spain

10. Genetics Area, Faculty of Medicine/IDINEUniversity of Castilla‐La Mancha Albacete Spain

Publisher

Wiley

Subject

Ophthalmology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ceo.13532

Reference31 articles.

1. Genetics of the Corneal Dystrophies

2. Corneal dystrophies

3. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

4. IC3D Classification of Corneal Dystrophies—Edition 2

5. Clinical and Genetic Aspects of the TGFBI-associated Corneal Dystrophies

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