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Analysis of rare variants in the CFH gene in patients with the cuticular drusen subtype of age-related macular degeneration.
Duvvari, Maheswara R; Saksens, Nicole T M; van de Ven, Johannes P H; de Jong-Hesse, Yvonne; Schick, Tina; Nillesen, Willy M; Fauser, Sascha; Hoefsloot, Lies H; Hoyng, Carel B; de Jong, Eiko K; den Hollander, Anneke I.
Affiliation
  • Duvvari MR; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, the Netherlands ; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Saksens NT; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • van de Ven JP; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • de Jong-Hesse Y; Department of Ophthalmology, VU Medical Centre, Amsterdam, the Netherlands.
  • Schick T; Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany.
  • Nillesen WM; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Fauser S; Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany.
  • Hoefsloot LH; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands ; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, the Netherlands.
  • Hoyng CB; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • de Jong EK; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, the Netherlands ; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • den Hollander AI; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, the Netherlands ; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands.
Mol Vis ; 21: 285-92, 2015.
Article in En | MEDLINE | ID: mdl-25814826
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Eye Diseases, Hereditary / Retinal Drusen / Bruch Membrane / Complement Factor H / Polymorphism, Single Nucleotide / Macular Degeneration Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2015 Document type: Article Affiliation country: Netherlands Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Eye Diseases, Hereditary / Retinal Drusen / Bruch Membrane / Complement Factor H / Polymorphism, Single Nucleotide / Macular Degeneration Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2015 Document type: Article Affiliation country: Netherlands Country of publication: United States