Fujiki K، Nakayasu K، Kanai A (2001). "Corneal dystrophies in Japan". J. Hum. Genet. ج. 46 ع. 8: 431–5. DOI:10.1007/s100380170041. PMID:11501939.
Schmitt-Bernard CF، Pouliquen Y، Argilès A (2004). "[BIG-H3 protein: mutation of codon 124 and corneal amyloidosis]". Journal français d'ophtalmologie. ج. 27 ع. 5: 510–22. DOI:10.1016/S0181-5512(04)96173-6. PMID:15179309.
Pieramici SF، Afshari NA (2006). "Genetics of corneal dystrophies: the evolving landscape". Current Opinion in Ophthalmology. ج. 17 ع. 4: 361–6. DOI:10.1097/01.icu.0000233955.94347.84. PMID:16900028.
Skonier J، Neubauer M، Madisen L، وآخرون (1992). "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. ج. 11 ع. 7: 511–22. DOI:10.1089/dna.1992.11.511. PMID:1388724.
Skonier J، Bennett K، Rothwell V، وآخرون (1994). "beta ig-h3: a transforming growth factor-beta-responsive gene encoding a secreted protein that inhibits cell attachment in vitro and suppresses the growth of CHO cells in nude mice". DNA Cell Biol. ج. 13 ع. 6: 571–84. DOI:10.1089/dna.1994.13.571. PMID:8024701.
Escribano J، Hernando N، Ghosh S، وآخرون (1994). "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. ج. 160 ع. 3: 511–21. DOI:10.1002/jcp.1041600314. PMID:8077289.
Maruyama K، Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. ج. 138 ع. 1–2: 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID:8125298.
Hashimoto K، Noshiro M، Ohno S، وآخرون (1997). "Characterization of a cartilage-derived 66-kDa protein (RGD-CAP/beta ig-h3) that binds to collagen". Biochim. Biophys. Acta. ج. 1355 ع. 3: 303–14. DOI:10.1016/S0167-4889(96)00147-4. PMID:9061001.
Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، وآخرون (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. ج. 200 ع. 1–2: 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID:9373149.
Fujiki K، Hotta Y، Nakayasu K، وآخرون (1998). "A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities". Hum. Genet. ج. 103 ع. 3: 286–9. DOI:10.1007/s004390050818. PMID:9799082.
Stewart HS، Ridgway AE، Dixon MJ، وآخرون (1999). "Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis". Hum. Mutat. ج. 14 ع. 2: 126–32. DOI:10.1002/(SICI)1098-1004(1999)14:2<126::AID-HUMU4>3.0.CO;2-W. PMID:10425035.
Rozzo C، Fossarello M، Galleri G، وآخرون (2000). "A common beta ig-h3 gene mutation (delta f540) in a large cohort of Sardinian Reis Bücklers corneal dystrophy patients. Mutations in brief no. 180. Online". Hum. Mutat. ج. 12 ع. 3: 215–6. PMID:10660331.