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Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations.
Bugueno, Isaac Maximiliano; Rey, Tristan; Jimenez-Armijo, Alexandra; Kawczynski, Marzena; Kharouf, Naji; Manière, Marie-Cécile; Herault, Yann; Bloch-Zupan, Agnès; Haushalter-Laugel, Virginie.
Afiliación
  • Bugueno IM; Institute of Genetics and Molecular and Cellular Biology (IGBMC), CNRS- UMR7104, INSERM U1258, Université de Strasbourg, Illkirch 67400, France.
  • Rey T; Faculty of Dentistry, Université de Strasbourg, Strasbourg 67000, France.
  • Jimenez-Armijo A; Reference Center for Rare Oral and Dental Diseases (CRMR-O-Rares), Oral Medicine and Surgery Department, Hôpitaux Universitaires de Strasbourg (HUS), Strasbourg 67000, France.
  • Kawczynski M; Rare Diseases Health Network "TETE COU" & European Reference Network ERN CRANIO, Strasbourg 67000, France.
  • Kharouf N; Orofacial Development and Regeneration, Faculty of Medicine, Institute of Oral Biology, Centre of Dental Medicine, University of Zürich, Zürich 8032, Switzerland.
  • Manière MC; Institute of Genetics and Molecular and Cellular Biology (IGBMC), CNRS- UMR7104, INSERM U1258, Université de Strasbourg, Illkirch 67400, France.
  • Herault Y; "Institut de Génétique Médicale d'Alsace", Laboratory of Genetic Diagnostic, Hôpitaux Universitaires de Strasbourg (HUS), Strasbourg 67000, France.
  • Bloch-Zupan A; Institute of Genetics and Molecular and Cellular Biology (IGBMC), CNRS- UMR7104, INSERM U1258, Université de Strasbourg, Illkirch 67400, France.
  • Haushalter-Laugel V; Faculty of Dentistry, Université de Strasbourg, Strasbourg 67000, France.
Genes Dis ; 11(5): 101303, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38721411
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Genes Dis Año: 2024 Tipo del documento: Article País de afiliación: Francia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Genes Dis Año: 2024 Tipo del documento: Article País de afiliación: Francia