首页|Rare dentin defects:Understanding the pathophysiological mechanisms of COLXVA1 mutations

Rare dentin defects:Understanding the pathophysiological mechanisms of COLXVA1 mutations

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Isaac Maximiliano Bugueno、Tristan Rey、Alexandra Jimenez-Armijo、Marzena Kawczynski、Naji Kharouf、Marie-Cécile Manière、Yann Herault、Agnès Bloch-Zupan、Virginie Haushalter-Laugel

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Institute of Genetics and Molecular and Cellular Biology(IGBMC),CNRS-UMR7104,INSERM U1258,Université de Strasbourg,Illkirch 67400,France

Faculty of Dentistry,Université de Strasbourg,Strasbourg 67000,France

Reference Center for Rare Oral and Dental Diseases(CRMR-O-Rares),Oral Medicine and Surgery Department,Hôpitaux Universitaires de Strasbourg(HUS),Strasbourg 67000,France

Rare Diseases Health Network"TETE COU"& European Reference Network ERN CRANIO,Strasbourg 67000,France

Orofacial Development and Regenera

"Institut de Génétique Médicale d'Alsace",Laboratory of Genetic Diagnostic,Hôpitaux Universitaires de Strasbourg(HUS),Strasbourg 67000,France

Biomaterials and Bioengineering Laboratory,Inserm UMR_S 1121,Strasbourg 67000,France

Institute of Advanced Studies(USIAS),Université de Strasbourg,Strasbourg 67045,France

Rare Diseases Health Network"TETE COU"& European R

"Institut de Génétique Médicale d'Alsace",Laboratory of Genetic Diagnostic,Hôpitaux Universitaires de Strasbourg(HUS),Strasbourg 67000,F

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French State fund managed by the Agence Nationale de la Recherche under the frame programme Investissements d'Avenir labelledProjet E-GENODENT financed by the Fonds d'Intervention Régionale(FIR)of the Agence Régionale de Santé Grand Est(2019-2022)

ANR-10-IDEX-0002-02

2024

基因与疾病(英文)

基因与疾病(英文)

ISSN:
年,卷(期):2024.11(5)