Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration.
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| Title: | Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration. |
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| Authors: | Kremlitzka M; Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö Sweden., Geerlings MJ; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., de Jong S; Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö Sweden.; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Bakker B; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Nilsson SC; Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö Sweden., Fauser S; Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany.; F. Hoffmann-La Roche AG, Basel, Switzerland., Hoyng CB; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., de Jong EK; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., den Hollander AI; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Blom AM; Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö Sweden. |
| Source: | Human molecular genetics [Hum Mol Genet] 2018 Aug 01; Vol. 27 (15), pp. 2678-2688. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1460-2083 |
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| DOI: | 10.1093/hmg/ddy178 |
