Clinical characterization of posterior polymorphous corneal dystrophy in patients of Indian ethnicity
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/article/10.1007/s10792-016-0360-y/fulltext.html
Reference16 articles.
1. Cibis GW, Krachmer JA, Phelps CD, Weingeist TA (1977) The clinical spectrum of posterior polymorphous dystrophy. Arch Ophthalmol 95(9):1529–1537
2. Heon E et al (1995) Linkage of posterior polymorphous corneal dystrophy to 20q11. Hum Mol Genet 4(3):485–488
3. Biswas S et al (2001) Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy. Hum Mol Genet 10(21):2415–2423
4. Shimizu S et al (2004) A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome10. Am J Med Genet A 130A(4):372–377
5. Liskova P, Gwilliam R, Filipec M, Jirsova K, Reinstein Merjava S, Deloukas P et al (2012) High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation. PLoS One 7(9):e45495
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