Citations for
1KTCN1, VSX1
Contributions of VSX1 gene to keratoconus.
Kalasidou G, Frydas I, Kozei A, Syrmakesi P, Loukovitis E, Sfakianakis K, Balidis M, Zachariadis Z, Tranos P, Kozeis N, Anogeianakis G.
J Biol Regul Homeost Agents 32(6):1515-1518. 2018
2KTCN1, VSX1
Analysis of VSX1 Variations in Brazilian Subjects with Keratoconus.
da Silva DC, Gadelha BNB, Feitosa AFB, da Silva RG, Albuquerque TLPE, Santos DCPF, Gadelha DNB, Fonseca Schamber-Reis BL.
J Ophthalmic Vis Res 13(3):266-273. doi: 10.4103/jovr.jovr_116_17. 2018
3KTCN1, VSX1
Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.
Verma A, Das M, Srinivasan M, Prajna NV, Sundaresan P.
BMC Res Notes 6:103. doi: 10.1186/1756-0500-6-103. 2013
4KTCN1, VSX1
Mutational screening of VSX1 in keratoconus patients from the European population.
Dash DP, George S, O'Prey D, Burns D, Nabili S, Donnelly U, Hughes AE, Silvestri G, Jackson J, Frazer D, Héon E, Willoughby CE.
Eye (Lond) 24(6):1085-92. Epub 2009 Sep 18.PMID: 19763142 2010
5KTCN1, VSX1
A novel VSX1 mutation identified in an individual with keratoconus in India.
Paliwal P, Singh A, Tandon R, Titiyal JS, Sharma A.
Mol Vis 15:2475-9.PMID: 19956409 2009
6KTCN1, VSX1
VSX1 gene variants are associated with keratoconus in unrelated Korean patients.
Mok JW, Baek SJ, Joo CK.
J Hum Genet 53(9):842-9. Epub 2008 Jul 15. 2008
7ALX4, PFM1, MNX1, SCRA, VSX1, KTCN1, VSX2, MCIA, SOPT, HESX1, HOXD13, PSDY2, MSX2, PFM2, SIX3, HPE2, DCS, SHOX
Homeodomain revisited: a lesson from disease-causing mutations.
Chi YI.
Hum Genet 116(6):433-44. Epub 2005 Feb 23. 2005
8KTCN1, KTCN4, VSX1
VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation.
Bisceglia L, Ciaschetti M, De Bonis P, Campo PA, Pizzicoli C, Scala C, Grifa M, Ciavarella P, Delle Noci N, Vaira F, Macaluso C, Zelante L.
Invest Ophthalmol Vis Sci 46(1):39-45. 2005
9KTCN1
Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia.
Fullerton J, Paprocki P, Foote S, Mackey DA, Williamson R, Forrest S.
Hum Genet 110(5):462-70. 2002
10KTCN1, VSX1
VSX1: a gene for posterior polymorphous dystrophy and keratoconus.
Heon E, Greenberg A, Kopp KK, Rootman D, Vincent AL, Billingsley G, Priston M, Dorval KM, Chow RL, McInnes RR, Heathcote G, Westall C, Sutphin JE, Semina E, Bremner R, Stone EM.
Hum Mol Genet 11(9):1029-36. 2002