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Citation: Kn. Alagramam et al., Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F (vol 10, pg 1709, 2001), HUM MOL GEN, 10(22), 2001, pp. 2603-2603

Authors: Alagramam, KN Yuan, HJ Kuehn, MH Murcia, CL Wayne, S Srisailpathy, CRS Lowry, RB Knaus, R Van Laer, L Bernier, FP Schwartz, S Lee, C Morton, CC Mullins, RF Ramesh, A Van Camp, G Hagemen, GS Woychik, RP Smith, RJH

Citation: Kn. Alagramam et al., Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F, HUM MOL GEN, 10(16), 2001, pp. 1709-1718

Authors: Kuehn, MH Stone, EM Hageman, GS

Citation: Mh. Kuehn et al., Organization of the human IMPG2 gene and its evaluation as a candidate gene in age-related macular degeneration and other retinal degenerative disorders, INV OPHTH V, 42(13), 2001, pp. 3123-3129

Authors: Ruiz, A Kuehn, MH Andorf, JL Stone, E Hageman, GS Bok, D

Citation: A. Ruiz et al., Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium, INV OPHTH V, 42(1), 2001, pp. 31-37

Authors: Gorin, MB Breitner, JCS De Jong, PTVM Hageman, GS Klaver, CCW Kuehn, MH Seddon, JM

Citation: Mb. Gorin et al., The genetics of age-related macular degeneration, MOL VIS, 5(24-35), 1999, pp. NIL_31-NIL_36

Authors: Kuehn, MH Hageman, GS

Citation: Mh. Kuehn et Gs. Hageman, Expression and characterization of the IPM 150 gene (IMPG1) product, a novel human photoreceptor cell-associated chondroitin-sulfate proteoglycan, MATRIX BIOL, 18(5), 1999, pp. 509-518