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Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype.
Averdunk, Luisa; Sticht, Heinrich; Surowy, Harald; Lüdecke, Hermann-Josef; Koch-Hogrebe, Margarete; Alsaif, Hessa S; Kahrizi, Kimia; Alzaidan, Hamad; Alawam, Bashayer S; Tohary, Mohamed; Kraus, Cornelia; Endele, Sabine; Wadman, Erin; Kaplan, Julie D; Efthymiou, Stephanie; Najmabadi, Hossein; Reis, André; Alkuraya, Fowzan S; Wieczorek, Dagmar.
Afiliação
  • Averdunk L; Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Universitätsstraße 1, 40225, Düsseldorf, Germany.
  • Sticht H; Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.
  • Surowy H; Division of Bioinformatics, Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Lüdecke HJ; Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Universitätsstraße 1, 40225, Düsseldorf, Germany.
  • Koch-Hogrebe M; Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Universitätsstraße 1, 40225, Düsseldorf, Germany.
  • Alsaif HS; Children's Hospital Datteln, University Witten Herdecke, Datteln, Germany.
  • Kahrizi K; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alzaidan H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Alawam BS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Tohary M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Kraus C; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Endele S; Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Wadman E; Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Kaplan JD; Division of Medical Genetics, Department of Pediatrics, DuPont Hospital for Children, Nemours Alfred I, Wilmington, Delaware, DE, USA.
  • Efthymiou S; Division of Medical Genetics, Department of Pediatrics, DuPont Hospital for Children, Nemours Alfred I, Wilmington, Delaware, DE, USA.
  • Najmabadi H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, The National Hospital for Neurology and Neurosurgery, London, UK.
  • Reis A; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alkuraya FS; Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Wieczorek D; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
J Mol Med (Berl) ; 99(12): 1769-1770, 2021 Dec.
Article em En | MEDLINE | ID: mdl-34661688
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article