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A mouse model of brittle cornea syndrome caused by mutation in Zfp469.
Stanton, Chloe M; Findlay, Amy S; Drake, Camilla; Mustafa, Mohammad Z; Gautier, Philippe; McKie, Lisa; Jackson, Ian J; Vitart, Veronique.
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  • Stanton CM; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Findlay AS; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Drake C; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Mustafa MZ; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Gautier P; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • McKie L; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Jackson IJ; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Vitart V; MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
Dis Model Mech ; 14(9)2021 09 01.
Article en En | MEDLINE | ID: mdl-34368841
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Cutáneas / Proteínas de Unión al ADN Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Dis Model Mech Asunto de la revista: MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Cutáneas / Proteínas de Unión al ADN Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Dis Model Mech Asunto de la revista: MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Reino Unido