Corrigendum to "Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome" [Biochim. Biophys. Acta Mol. Basis Dis. 1872 (2026)/168184].
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| Title: | Corrigendum to "Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome" [Biochim. Biophys. Acta Mol. Basis Dis. 1872 (2026)/168184]. |
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| Authors: | Aynekin B; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK; Department of Molecular Biology and Genetics, Biruni University, 34015, Istanbul, Türkiye., Lau T; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Kaiyrzhanov R; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Papazoglou I; Laboratory for Innovative Drugs (Lab4IND), Computational Drug Design Center (HİTMER), Bahçeşehir University, 34734, İstanbul, Türkiye., Gulec A; Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey., Gumus UGO; Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey., Gorokhova S; Department of Medical Genetics, Timone Children's Hospital, APHM, Marseille, France., Tiffany B; Department of Medical Genetics, Timone Children's Hospital, APHM, Marseille, France., Medeiros LS; Medical Genetics Service-Hospital de Clinicas de Porto Alegre-Brazil, Porto Alegre, RS, Brazil., Schwartz IVD; Medical Genetics Service-Hospital de Clinicas de Porto Alegre-Brazil, Porto Alegre, RS, Brazil., Mutlu MB; Department of Medical Genetics, Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye., Ourani S; Clinical Genetics Department, Archbishop Makarios III Hospital, Nicosia, Cyprus., Bergman A; Hannover Medical School, Institute of Human Genetics, Hannover, Germany., Schoch K; Division of Medical Genetics, Pediatrics, Duke University School of Medicine, Durham, NC, USA., Per H; Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey., Bingol NN; Department of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, Bursa, Türkiye., Temel SG; Department of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, Bursa, Türkiye; Department of Medical Genetics, Faculty of Medicine, Bursa Uludag University, Bursa, Türkiye; Department of Histology and Embryology, Faculty of Medicine, Bursa Uludag University, Bursa, Türkiye., Durdağı S; Laboratory for Innovative Drugs (Lab4IND), Computational Drug Design Center (HİTMER), Bahçeşehir University, 34734, İstanbul, Türkiye; Molecular Therapy Lab, Department of Pharmaceutical Chemistry, School of Pharmacy, Bahcesehir University, Istanbul, Türkiye; Systems Biology Lab, Biruni University Scientific Research Center, Biruni University, Istanbul, Türkiye. Electronic address: serdar.durdagi@bau.edu.tr., Hız S; Department of Pediatric Neurology, Faculty of Medicine, Dokuz Eylül University, Izmir, 35340, Turkey., Bernard G; Department of Neurology and Neurosurgery, McGill University, Montreal, Canada; Department of Pediatrics, McGill University, Montreal, Canada; Child Health and Human Development Program, McGill University Health Centre Research Institute, Montreal, Canada; Department Specialized Medicine, Division of Medical Genetics, McGill University Health Centre, Montreal, Canada; Department of Human Genetics, McGill University, Montreal, Canada., Tobon FV; Department of Neurology and Neurosurgery, McGill University, Montreal, Canada., Houlden H; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Electronic address: h.houlden@ucl.ac.uk., Efthymiou S; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Electronic address: s.efthymiou@ucl.ac.uk. |
| Source: | Biochimica et biophysica acta. Molecular basis of disease [Biochim Biophys Acta Mol Basis Dis] 2026 Jun; Vol. 1872 (5), pp. 168222. Date of Electronic Publication: 2026 Mar 11. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101731730 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-260X (Electronic) Linking ISSN: 09254439 NLM ISO Abbreviation: Biochim Biophys Acta Mol Basis Dis Subsets: MEDLINE; In Process |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41820113 AccessLevel: 2 PubTypeId: unknown PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Corrigendum to "Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome" [Biochim. Biophys. Acta Mol. Basis Dis. 1872 (2026)/168184]. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Aynekin+B%22">Aynekin B</searchLink>; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK; Department of Molecular Biology and Genetics, Biruni University, 34015, Istanbul, Türkiye.<br /><searchLink fieldCode="AU" term="%22Lau+T%22">Lau T</searchLink>; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Kaiyrzhanov+R%22">Kaiyrzhanov R</searchLink>; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Papazoglou+I%22">Papazoglou I</searchLink>; Laboratory for Innovative Drugs (Lab4IND), Computational Drug Design Center (HİTMER), Bahçeşehir University, 34734, İstanbul, Türkiye.<br /><searchLink fieldCode="AU" term="%22Gulec+A%22">Gulec A</searchLink>; Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey.<br /><searchLink fieldCode="AU" term="%22Gumus+UGO%22">Gumus UGO</searchLink>; Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey.<br /><searchLink fieldCode="AU" term="%22Gorokhova+S%22">Gorokhova S</searchLink>; Department of Medical Genetics, Timone Children's Hospital, APHM, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Tiffany+B%22">Tiffany B</searchLink>; Department of Medical Genetics, Timone Children's Hospital, APHM, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Medeiros+LS%22">Medeiros LS</searchLink>; Medical Genetics Service-Hospital de Clinicas de Porto Alegre-Brazil, Porto Alegre, RS, Brazil.<br /><searchLink fieldCode="AU" term="%22Schwartz+IVD%22">Schwartz IVD</searchLink>; Medical Genetics Service-Hospital de Clinicas de Porto Alegre-Brazil, Porto Alegre, RS, Brazil.<br /><searchLink fieldCode="AU" term="%22Mutlu+MB%22">Mutlu MB</searchLink>; Department of Medical Genetics, Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye.<br /><searchLink fieldCode="AU" term="%22Ourani+S%22">Ourani S</searchLink>; Clinical Genetics Department, Archbishop Makarios III Hospital, Nicosia, Cyprus.<br /><searchLink fieldCode="AU" term="%22Bergman+A%22">Bergman A</searchLink>; Hannover Medical School, Institute of Human Genetics, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Schoch+K%22">Schoch K</searchLink>; Division of Medical Genetics, Pediatrics, Duke University School of Medicine, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22Per+H%22">Per H</searchLink>; Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey.<br /><searchLink fieldCode="AU" term="%22Bingol+NN%22">Bingol NN</searchLink>; Department of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, Bursa, Türkiye.<br /><searchLink fieldCode="AU" term="%22Temel+SG%22">Temel SG</searchLink>; Department of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, Bursa, Türkiye; Department of Medical Genetics, Faculty of Medicine, Bursa Uludag University, Bursa, Türkiye; Department of Histology and Embryology, Faculty of Medicine, Bursa Uludag University, Bursa, Türkiye.<br /><searchLink fieldCode="AU" term="%22Durdağı+S%22">Durdağı S</searchLink>; Laboratory for Innovative Drugs (Lab4IND), Computational Drug Design Center (HİTMER), Bahçeşehir University, 34734, İstanbul, Türkiye; Molecular Therapy Lab, Department of Pharmaceutical Chemistry, School of Pharmacy, Bahcesehir University, Istanbul, Türkiye; Systems Biology Lab, Biruni University Scientific Research Center, Biruni University, Istanbul, Türkiye. Electronic address: serdar.durdagi@bau.edu.tr.<br /><searchLink fieldCode="AU" term="%22Hız+S%22">Hız S</searchLink>; Department of Pediatric Neurology, Faculty of Medicine, Dokuz Eylül University, Izmir, 35340, Turkey.<br /><searchLink fieldCode="AU" term="%22Bernard+G%22">Bernard G</searchLink>; Department of Neurology and Neurosurgery, McGill University, Montreal, Canada; Department of Pediatrics, McGill University, Montreal, Canada; Child Health and Human Development Program, McGill University Health Centre Research Institute, Montreal, Canada; Department Specialized Medicine, Division of Medical Genetics, McGill University Health Centre, Montreal, Canada; Department of Human Genetics, McGill University, Montreal, Canada.<br /><searchLink fieldCode="AU" term="%22Tobon+FV%22">Tobon FV</searchLink>; Department of Neurology and Neurosurgery, McGill University, Montreal, Canada.<br /><searchLink fieldCode="AU" term="%22Houlden+H%22">Houlden H</searchLink>; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Electronic address: h.houlden@ucl.ac.uk.<br /><searchLink fieldCode="AU" term="%22Efthymiou+S%22">Efthymiou S</searchLink>; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Electronic address: s.efthymiou@ucl.ac.uk. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101731730%22">Biochimica et biophysica acta. Molecular basis of disease</searchLink> [Biochim Biophys Acta Mol Basis Dis] 2026 Jun; Vol. 1872 (5), pp. 168222. <i>Date of Electronic Publication: </i>2026 Mar 11. – Name: TypePub Label: Publication Type Group: TypPub Data: Published Erratum – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>Netherlands <i>NLM ID: </i>101731730 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1879-260X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209254439%22">09254439 </searchLink><i>NLM ISO Abbreviation: </i>Biochim Biophys Acta Mol Basis Dis <i>Subsets: </i>MEDLINE; In Process |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41820113 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.bbadis.2026.168222 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 168222 Titles: – TitleFull: Corrigendum to "Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome" [Biochim. Biophys. Acta Mol. Basis Dis. 1872 (2026)/168184]. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Aynekin B – PersonEntity: Name: NameFull: Lau T – PersonEntity: Name: NameFull: Kaiyrzhanov R – PersonEntity: Name: NameFull: Papazoglou I – PersonEntity: Name: NameFull: Gulec A – PersonEntity: Name: NameFull: Gumus UGO – PersonEntity: Name: NameFull: Gorokhova S – PersonEntity: Name: NameFull: Tiffany B – PersonEntity: Name: NameFull: Medeiros LS – PersonEntity: Name: NameFull: Schwartz IVD – PersonEntity: Name: NameFull: Mutlu MB – PersonEntity: Name: NameFull: Ourani S – PersonEntity: Name: NameFull: Bergman A – PersonEntity: Name: NameFull: Schoch K – PersonEntity: Name: NameFull: Per H – PersonEntity: Name: NameFull: Bingol NN – PersonEntity: Name: NameFull: Temel SG – PersonEntity: Name: NameFull: Durdağı S – PersonEntity: Name: NameFull: Hız S – PersonEntity: Name: NameFull: Bernard G – PersonEntity: Name: NameFull: Tobon FV – PersonEntity: Name: NameFull: Houlden H – PersonEntity: Name: NameFull: Efthymiou S IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 2026 Jun Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1879-260X Numbering: – Type: volume Value: 1872 – Type: issue Value: 5 Titles: – TitleFull: Biochimica et biophysica acta. Molecular basis of disease Type: main |
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