Author Correction: The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.
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| Title: | Author Correction: The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture. |
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| Authors: | Vazquez N; Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA., Lee C; Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA., Valenzuela I; Department of Pediatrics, Faculty of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain.; Department of Clinical and Molecular Genetics, Vall d´Hebron University Hospital. European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Medicine Genetics Group, Vall d´Hebron Research Institute, Barcelona, Spain., Phan TP; Department of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA., Derderian C; Department of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA., Chávez M; Baxter Laboratory, Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, USA., Mooney NA; Baxter Laboratory, Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, USA., Demeter J; Baxter Laboratory, Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, USA., Aziz-Zanjani MO; Baxter Laboratory, Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, USA., Cusco I; Department of Clinical and Molecular Genetics, Vall d´Hebron University Hospital. European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Medicine Genetics Group, Vall d´Hebron Research Institute, Barcelona, Spain., Codina M; Department of Clinical and Molecular Genetics, Vall d´Hebron University Hospital. European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Medicine Genetics Group, Vall d´Hebron Research Institute, Barcelona, Spain., Martínez-Gil N; Department of Clinical and Molecular Genetics, Vall d´Hebron University Hospital. European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Medicine Genetics Group, Vall d´Hebron Research Institute, Barcelona, Spain., Valverde D; CINBIO, University of Vigo and Research Group on Rare Diseases and Pediatric Medicine, Health Research Institute Galicia Sur (IIS Galicia Sur), SERGASUVIGO, Vigo, Spain., Solarat C; CINBIO, University of Vigo and Research Group on Rare Diseases and Pediatric Medicine, Health Research Institute Galicia Sur (IIS Galicia Sur), SERGASUVIGO, Vigo, Spain., Bruel AL; Functional Unity of Innovative Diagnosis for Rare Diseases and Inserm UMR1231 team GAD, University of Burgundy, Dijon, France., Thauvin-Robinet C; Functional Unity of Innovative Diagnosis for Rare Diseases and Inserm UMR1231 team GAD, University of Burgundy, Dijon, France., Steichen E; Department of Pediatrics, Medical School, University of Innsbruck, Innsbruck, Austria., Filges I; Medical Genetics, Institute of Medical Genetics and Pathology and Department of Clinical Research, University Hospital Basel, Basel, Switzerland., Joset P; Medical Genetics, Institute of Medical Genetics and Pathology and Department of Clinical Research, University Hospital Basel, Basel, Switzerland., De Geyter J; Medical Genetics, Institute of Medical Genetics and Pathology and Department of Clinical Research, University Hospital Basel, Basel, Switzerland., Vaidyanathan K; Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA., Gardner TP; Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA., Toriyama M; Department of Biomedical Sciences, School of Biological and Environmental Sciences, Kwansei Gakuin University, Sanda, Hyogo, Japan., Marcotte EM; Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA., Drew K; Department of Biological Sciences, University of Illinois at Chicago, Chicago, IL, USA., Roberson EC; Developmental Biology and Pediatrics, CU Anschutz Medical Campus, Aurora, CO, USA., Jackson PK; Baxter Laboratory, Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, USA., Reiter JF; Department of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA., Tizzano EF; Department of Clinical and Molecular Genetics, Vall d´Hebron University Hospital. European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Medicine Genetics Group, Vall d´Hebron Research Institute, Barcelona, Spain. eduardo.tizzano@vallhebron.cat., Wallingford JB; Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA. wallingford@utexas.edu. |
| Source: | Nature communications [Nat Commun] 2026 Feb 02; Vol. 17 (1), pp. 1210. Date of Electronic Publication: 2026 Feb 02. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE; In Process |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2041-1723 |
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| DOI: | 10.1038/s41467-026-69058-z |
