PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Korean Journal of Ophthalmology10.3341/kjo.2014.28.1.83201428183A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in theTGFBIGeneJinsun Kim, Kyung A Lee, Eung Kweon Kim, Hyung Keun Leehttps://synapse.koreamed.org/DOIx.php?id=10.3341/kjo.2014.28.1.83, https://synapse.koreamed.org/pdf/10.3341/kjo.2014.28.1.83, http://synapse.koreamed.org/DOIx.php?id=10.3341/kjo.2014.28.1.83
Japanese Journal of Ophthalmology10.1016/s0021-5155(02)00644-5200347113-17A Novel Nonsense Mutation with a Compound Heterozygous Mutation in TGFBI Gene in Lattice Corneal Dystrophy Type IT Sakimotohttps://api.elsevier.com/content/article/PII:S0021-5155(02)00644-5?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0021-5155(02)00644-5?httpAccept=text/plain
Ophthalmic and Physiological Optics10.1111/j.1475-1313.2011.00867.x201132174-80TGFBI gene mutation in a Chinese pedigree with Reis-Bücklers corneal dystrophyQingfeng Liang, Xuguang Sun, Xiuying Jinhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1475-1313.2011.00867.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1475-1313.2011.00867.x/fullpdf
Japanese Journal of Ophthalmology10.1007/s10384-005-0260-6200650162-64Lattice Corneal Dystrophy Type III in Patients with a Homozygous L527R Mutation in the TGFBI GeneTomoyo Funayama, Yukihiko Mashima, Motoko Kawashima, Masakazu Yamadahttp://link.springer.com/content/pdf/10.1007/s10384-005-0260-6.pdf, http://link.springer.com/article/10.1007/s10384-005-0260-6/fulltext.html, http://link.springer.com/content/pdf/10.1007/s10384-005-0260-6
Yearbook of Ophthalmology10.1016/s0084-392x(09)79017-320092009234-235A Novel Variant of Combined Granular-Lattice Corneal Dystrophy Associated With the Met619Lys Mutation in the TGFBI GeneR.C. Eaglehttps://api.elsevier.com/content/article/PII:S0084392X09790173?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0084392X09790173?httpAccept=text/plain
Japanese Journal of Ophthalmology10.1007/s10384-010-0882-12010546628-629A case of lattice corneal dystrophy due to L527R mutation in the TGFBI gene with asymmetric corneal opacity in eye lateralityTakako Ohnishi, Tohru Sakimoto, Mitsuru Sawahttp://link.springer.com/content/pdf/10.1007/s10384-010-0882-1.pdf, http://link.springer.com/article/10.1007/s10384-010-0882-1/fulltext.html, http://link.springer.com/content/pdf/10.1007/s10384-010-0882-1
Acta Ophthalmologica10.1111/j.1755-3768.2010.2346.x201088s2460-0Novel mutation in the TGFBI gene in a patient with a late‐onset lattice corneal dystrophyM OLDAK, JP SZAFLIK, RB MAKSYM, M UDZIELA, M FRANASZCZYK, R PIOSKI, J SZAFLIKhttp://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1755-3768.2010.2346.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1755-3768.2010.2346.x/fullpdf
Acta Ophthalmologica10.1111/aos.13972_197201896S26155-56A possible novel TGFBI mutation Ser591Phe in a Finnish family with lattice corneal dystrophyhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/aos.13972_197, https://onlinelibrary.wiley.com/doi/full-xml/10.1111/aos.13972_197, https://onlinelibrary.wiley.com/doi/pdf/10.1111/aos.13972_197
Japanese Journal of Ophthalmology10.1007/s10384-004-0167-7200549284-88Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type IXin Tian, Keiko Fujiki, Wei Wang, Akira Murakami, Peiying Xie, Atsushi Kanai, Zuguo Liuhttp://link.springer.com/content/pdf/10.1007/s10384-004-0167-7.pdf, http://link.springer.com/article/10.1007/s10384-004-0167-7/fulltext.html, http://link.springer.com/content/pdf/10.1007/s10384-004-0167-7
Journal of Clinical Medicine10.3390/jcm11113055202211113055De Novo L509P Mutation of the TGFBI Gene Associated with Slit-Lamp Findings of Lattice Corneal Dystrophy Type IIIAYong Woo Ji, Hyunmin Ahn, Kyoung-Jin Shin, Tae-im Kim, Kyoung Yul Seo, R. Doyle Stulting, Eung Kweon Kimhttps://www.mdpi.com/2077-0383/11/11/3055/pdf