| 1 | GLC3D, LTBP2 |
| Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma. | |
| Chen X, Chen Y, Fan BJ, Xia M, Wang L, Sun X. | |
| Mol Vis 22:528-35. eCollection 2016. 2016 | |
| 2 | GLC3D, LTBP2 |
| Null mutations in LTBP2 cause primary congenital glaucoma. | |
| Ali M, McKibbin M, Booth A, Parry DA, Jain P, Riazuddin SA, Hejtmancik JF, Khan SN, Firasat S, Shires M, Gilmour DF, Towns K, Murphy AL, Azmanov D, Tournev I, Cherninkova S, Jafri H, Raashid Y, Toomes C, Craig J, Mackey DA, Kalaydjieva L, Riazuddin S, Inglehearn CF. | |
| Am J Hum Genet 84(5):664-71. Epub 2009 Apr 9. 2009 | |
| 3 | GLC3D, LTBP2 |
| Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma. | |
| Narooie-Nejad M, Paylakhi SH, Shojaee S, Fazlali Z, Rezaei Kanavi M, Nilforushan N, Yazdani S, Babrzadeh F, Suri F, Ronaghi M, Elahi E, Paisán-Ruiz C. | |
| Hum Mol Genet 18(20):3969-77. Epub 2009 Aug 4.PMID: 19656777 2009 | |