Authors: Thompson, DA McHenry, CL Li, Y Richards, JE Othman, MI Schwinger, E Vollrath, D Jacobson, SG Gal, A

Citation: Da. Thompson et al., Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome2, with homoallelism for mutations in RPE65 or MERTK, respectively, AM J HU GEN, 70(1), 2002, pp. 224-229

Authors: Thompson, DA Li, Y McHenry, CL Carlson, TJ Ding, X Sieving, PA Apfelstedt-Sylla, E Gal, A

Citation: Da. Thompson et al., Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy, NAT GENET, 28(2), 2001, pp. 123-124

Authors: Sieving, PA Fowler, ML Bush, RA Machida, S Calvert, PD Green, DG Makino, CL McHenry, CL

Citation: Pa. Sieving et al., Constitutive "light" adaptation in rods from G90D rhodopsin: A mechanism for human congenital nightblindness without rod cell loss, J NEUROSC, 21(15), 2001, pp. 5449-5460

Authors: Thompson, DA Gyurus, P Fleischer, LL Bingham, EL McHenry, CL Apfelstedt-Sylla, E Zrenner, E Lorenz, B Richards, JE Jacobson, SG Sieving, PA Gal, A

Citation: Da. Thompson et al., Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration, INV OPHTH V, 41(13), 2000, pp. 4293-4299