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- W3186962859 abstract "In the above-stated article, the given name and surname one of the authors, Erik Ilsoe Christensen, was presented inaccurately. The given name is Erik and the surname is Ilsoe Christensen. In addition, an additional affiliation of Maike Marczenke was omitted. The additional affiliation is the Department of Biology, Chemistry and Pharmacy, Freie Universitaet Berlin, Berlin, Germany. The authors would like to apologize for any inconvenience caused. Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndromeKidney InternationalVol. 98Issue 1PreviewDonnai-Barrow syndrome (DBS) is an autosomal-recessive disorder characterized by multiple pathologies including malformation of forebrain and eyes, as well as resorption defects of the kidney proximal tubule. The underlying cause of DBS are mutations in LRP2, encoding the multifunctional endocytic receptor megalin. Here, we identified a unique missense mutation R3192Q of LRP2 in an affected family that may provide novel insights into the molecular causes of receptor dysfunction in the kidney proximal tubule and other tissues affected in DBS. Full-Text PDF Open Access" @default.
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- W3186962859 date "2021-08-01" @default.
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- W3186962859 title "Corrigendum to Flemming J, Marczenke M, Rudolph I-M, et al. Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome. Kidney Int. 2020;98:159–167" @default.
- W3186962859 doi "https://doi.org/10.1016/j.kint.2021.06.014" @default.
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