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The EMBO Journal|April 3, 2002
Lack of collagen XVIII/endostatin results in eye abnormalitiesNaomi Fukai, Lauri Eklund, Alexander G Marneros, et al.Human Mutation|December 26, 2003
Knobloch syndrome: novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatinOlivier Menzel, Reidunn C J Bekkeheien, Alexandre Reymond, et al.The EMBO Journal|December 20, 2003
Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial functionAlexander G Marneros, Douglas R Keene, Uwe Hansen, et al.Pageof 3