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CFAP300 mutation causing primary ciliary dyskinesia in Finland.
Schultz, Rüdiger; Elenius, Varpu; Fassad, Mahmoud R; Freke, Grace; Rogers, Andrew; Shoemark, Amelia; Koistinen, Tiina; Mohamed, Mai A; Lim, Jacqueline S Y; Mitchison, Hannah M; Sironen, Anu I.
Afiliación
  • Schultz R; Allergy Centre, Tampere University Hospital, Tampere, Finland.
  • Elenius V; Department of Pediatrics, Turku University Hospital, University of Turku, Turku, Finland.
  • Fassad MR; Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
  • Freke G; Human Genetics Department, Medical Research Institute, Alexandria University, Alexandria, Egypt.
  • Rogers A; Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
  • Shoemark A; PCD Diagnostic Team and Department of Paediatric Respiratory Medicine, Royal Brompton Hospita, London, United Kingdom.
  • Koistinen T; PCD Diagnostic Team and Department of Paediatric Respiratory Medicine, Royal Brompton Hospita, London, United Kingdom.
  • Mohamed MA; School of Medicine, University of Dundee, Dundee, United Kingdom.
  • Lim JSY; Department of Otorhinolaryngology, Head and Neck Surgery, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland.
  • Mitchison HM; Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
  • Sironen AI; Biochemistry Division, Chemistry Department, Faculty of Science, Zagazig University, Zagazig, Egypt.
Front Genet ; 13: 985227, 2022.
Article en En | MEDLINE | ID: mdl-36246608
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Genet Año: 2022 Tipo del documento: Article País de afiliación: Finlandia Pais de publicación: Suiza
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Genet Año: 2022 Tipo del documento: Article País de afiliación: Finlandia Pais de publicación: Suiza