Mutation Hot Spots in 5q31-Linked Corneal Dystrophies-Reference-Cited by-同舟云学术

Mutation Hot Spots in 5q31-Linked Corneal Dystrophies

Published:1998-02 Issue:2 Volume:62 Page:320-324
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Korvatska E.,Munier F.L.,Djemaï A.,Wang M.X.,Frueh B.,Chiou A.G.-Y.,Uffer S.,Ballestrazzi E.,Braunstein R.E.,Forster R.K.,Culbertson W.W.,Boman H.,Zografos L.,Schorderet D.F.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Clinically atypical granular corneal dystrophy with pathologic features of lattice-like amyloid deposits—a study of three families;Folberg;Ophthalmology,1988

2. βig-h3 is synthesized by corneal epithelium and perhaps endothelium in Fuchs' dystrophic corneas;Hirano;Curr Eye Res,1996

3. Lattice corneal dystrophy: an inherited variety of amyloidosis restricted to the cornea;Klintworth;Am J Pathol,1967

4. Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX;Korvatska;Eur J Hum Genet,1996

5. Reevaluation of corneal dystrophies of Bowman's layer and the anterior stroma (Reis-Bücklers and Thiel-Behnke types): a light and electron microscopic study of eight corneas and a review of the literature;Küchle;Cornea,1995

Cited by 107 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Early Detection of Subclinical Corneal Abnormalities: Biophotonic Imaging Reveals Hyporeflective Bleb-Like Structures in Asymptomatic Eyes;American Journal of Case Reports;2024-07-17

2. Mini-Review: Clinical Features and Management of Granular Corneal Dystrophy Type 2;Korean Journal of Ophthalmology;2023-08-05

3. Corneal stromal dystrophies;Ophthalmic Pathology;2023

4. TMAO to the rescue of pathogenic protein variants;Biochimica et Biophysica Acta (BBA) - General Subjects;2022-11

5. Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort;Molecular Genetics & Genomic Medicine;2022-08-19