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Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Töpf, Ana; Griffin, Helen R; Glen, Elise; Soemedi, Rachel; Brown, Danielle L; Hall, Darroch; Rahman, Thahira J; Eloranta, Jyrki J; Jüngst, Christoph; Stuart, A Graham; O'Sullivan, John; Keavney, Bernard D; Goodship, Judith A.
Affiliation
  • Töpf A; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Griffin HR; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Glen E; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Soemedi R; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Brown DL; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Hall D; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Rahman TJ; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Eloranta JJ; Department of Clinical Pharmacology and Toxicology, University Hospital Zurich, Zurich, Switzerland.
  • Jüngst C; Department of Clinical Pharmacology and Toxicology, University Hospital Zurich, Zurich, Switzerland; Department of Medicine II, Saarland University Medical Center, Homburg, Germany.
  • Stuart AG; Bristol Royal Hospital for Children, Bristol, United Kingdom.
  • O'Sullivan J; Paediatric Cardiology, Freeman Hospital Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
  • Keavney BD; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom; Institute of Cardiovascular Sciences, The University of Manchester, Manchester, United Kingdom.
  • Goodship JA; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
PLoS One ; 9(8): e95453, 2014.
Article in En | MEDLINE | ID: mdl-25093829
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tetralogy of Fallot / Transcription Factors / Mutation Type of study: Prognostic_studies Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2014 Document type: Article Affiliation country: United kingdom Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tetralogy of Fallot / Transcription Factors / Mutation Type of study: Prognostic_studies Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2014 Document type: Article Affiliation country: United kingdom Country of publication: United States