1. Bron AJ, Aldave A, Akhtar S, et al. Tasman W, Jaeger EA, editors. Inherited dystrophies and developmental anomalies of the cornea. Duane's Ophthalmology. 2008. 2009 ed. Philadelphia: Lippincott Williams & Wilkins.
2. Jones ST, Zimmerman LE. Histopathologic differentiation of granular, macular and lattice dystrophies of the cornea. Am J Ophthalmol. 1961. 51:394–410.
3. Jones ST, Zimmerman LE. Macular dystrophy of the cornea (Groenouw type II); clinicopathologic report of two cases with comments concerning its differential diagnosis from lattice dystrophy (Biber-Haab-Dimmer). Am J Ophthalmol. 1959. 47(1 Part 1):1–16.
4. Weiss JS, Møller HU, Lisch W, et al. The IC3D classification of the corneal dystrophies. Cornea. 2008. 27:Suppl 2. S1–S83.
5. Møller HU, Weiss JS. IC3D classification of corneal dystrophies. Dev Ophthalmol. 2011. 48:1–8.
6. Al-Swailem SA, Al-Rajhi AA, Wagoner MD. Penetrating keratoplasty for macular corneal dystrophy. Ophthalmology. 2005. 112:220–224.
7. Akama TO, Nishida K, Nakayama J, et al. Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene. Nat Genet. 2000. 26:237–241.
8. Malbran ES. Macular corneal dystrophy in Saudi Arabia: a study of 56 cases and recognition of a new immunophenotype. Am J Ophthalmol. 1998. 125:417–418.
9. Jonasson F, Oshima E, Thonar EJ, et al. Macular corneal dystrophy in Iceland. A clinical, genealogic, and immunohistochemical study of 28 patients. Ophthalmology. 1996. 103:1111–1117.
10. Cho YA, Kim MH, Oh JS. A case of macular dystrophy of the cornea. J Korean Ophthalmol Soc. 1976. 17:217–221.
11. Kim IS, Myong YW. Cases of macular corneal dystrophy with a family history. J Korean Ophthalmol Soc. 1995. 36:874–878.
12. Skonier J, Neubauer M, Madisen L, et al. cDNA cloning and sequence analysis of beta ig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-beta. DNA Cell Biol. 1992. 11:511–522.
13. Zhang T, Yan N, Yu W, et al. Molecular genetics of Chinese families with TGFBI corneal dystrophies. Mol Vis. 2011. 17:380–387.
14. Escribano J, Hernando N, Ghosh S, et al. cDNA from human ocular ciliary epithelium homologous to beta ig-h3 is preferentially expressed as an extracellular protein in the corneal epithelium. J Cell Physiol. 1994. 160:511–521.
15. El Kochairi I, Letovanec I, Uffer S, et al. Systemic investigation of keratoepithelin deposits in TGFBI/BIGH3-related corneal dystrophy. Mol Vis. 2006. 12:461–466.
16. Yao YF, Jin YQ, Zhang B, et al. Recurrence of lattice corneal dystrophy caused by incomplete removal of stroma after deep lamellar keratoplasty. Cornea. 2006. 25:10 Suppl 1. S41–S46.
17. Meisler DM, Fine M. Recurrence of the clinical signs of lattice corneal dystrophy (type I) in corneal transplants. Am J Ophthalmol. 1984. 97:210–214.
18. Lyons CJ, McCartney AC, Kirkness CM, et al. Granular corneal dystrophy. Visual results and pattern of recurrence after lamellar or penetrating keratoplasty. Ophthalmology. 1994. 101:1812–1817.
19. Adamis AP, Filatov V, Tripathi BJ, Tripathi RC. Fuchs' endothelial dystrophy of the cornea. Surv Ophthalmol. 1993. 38:149–168.
20. Pineros O, Cohen EJ, Rapuano CJ, Laibson PR. Long-term results after penetrating keratoplasty for Fuchs' endothelial dystrophy. Arch Ophthalmol. 1996. 114:15–18.
21. Happ DM, Lewis DA, Eng KH, et al. Postoperative visual acuity in patients with fuchs dystrophy undergoing descemet membrane-stripping automated endothelial keratoplasty: correlation with the severity of histologic changes. Arch Ophthalmol. 2012. 130:33–38.
22. Lee HS, Kim MS. Influential factors on the survival of endothelial cells after penetrating keratoplasty. Eur J Ophthalmol. 2009. 19:930–935.
23. Langenbucher A, Seitz B, Nguyen NX, Naumann GO. Corneal endothelial cell loss after nonmechanical penetrating keratoplasty depends on diagnosis: a regression analysis. Graefes Arch Clin Exp Ophthalmol. 2002. 240:387–392.
24. Yellore VS, Rayner SA, Aldave AJ. TGFB1-induced extracellular expression of TGFBIp and inhibition of TGFBIp expression by RNA interference in a human corneal epithelial cell line. Invest Ophthalmol Vis Sci. 2011. 52:757–763.
25. Aldave AJ, Sonmez B, Forstot SL, et al. A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy. Am J Ophthalmol. 2007. 143:416–419.
26. Kannabiran C, Klintworth GK. TGFBI gene mutations in corneal dystrophies. Hum Mutat. 2006. 27:615–625.
27. Klintworth GK, Reed J, Stainer GA, Binder PS. Recurrence of macular corneal dystrophy within grafts. Am J Ophthalmol. 1983. 95:60–72.
28. Akova YA, Kirkness CM, McCartney AC, et al. Recurrent macular corneal dystrophy following penetrating keratoplasty. Eye (Lond). 1990. 4(Pt 5):698–705.