C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
2007 · Nature Genetics · 444 citations
https://doi.org/10.1038/ng2082
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Andreas Gschwendter is an academic researcher from Ludwig-Maximilians-Universität München. The author has contributed to research in topics: Ocular Diseases and Behçet’s Syndrome & Retinal Diseases and Treatments & Neutrophil, Myeloperoxidase and Oxidative Mechanisms. The author has an h-index of 2, co-authored 2 publications.
https://doi.org/10.1038/ng2082
https://doi.org/10.1093/brain/aww217
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