Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions
Author:
Publisher
MDPI AG
Subject
Genetics(clinical),Genetics
Link
http://www.mdpi.com/2073-4425/8/7/170/pdf
Reference22 articles.
1. Hyaluronan and the functional organization of the interphotoreceptor matrix;Hollyfield;Investig. Ophthalmol. Vis. Sci.,1999
2. Structure and function of the interphotoreceptor matrix surrounding retinal photoreceptor cells
3. Proteoglycans in retina
4. The Benign Concentric Annular Macular Dystrophy Locus Maps to 6p12.3-q16
5. Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa
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1. IMPG2-Related Maculopathy;American Journal of Ophthalmology;2024-02
2. Early Macular Involvement in Non-syndromic Retinitis Pigmentosa;Macular Diseases - An Update [Working Title];2023-12-06
3. Heterogeneity in the progression of retinal pathologies in mice harboring patient mimicking Impg2 mutations;Human Molecular Genetics;2023-11-17
4. Novel IMPG2 variant causing adult macular vitelliform dystrophy: A case report;European Journal of Ophthalmology;2023-09-03
5. Identification of the zebrafish homologues of IMPG2, a retinal proteoglycan;Cell and Tissue Research;2023-07-20
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