SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects
Johanne Dubail(Délégation Paris 5), Valérie Cormier‐Daire(Institut Necker Enfants Malades), Irene Stolte‐Dijkstra(University of Groningen), Jeanne Amiel(Hôpital Necker-Enfants Malades), Arnold Münnich(Hôpital Necker-Enfants Malades), Koen L.I. van Gassen(University Medical Center Utrecht), Céline Huber(Délégation Paris 5), Elisabeth Steichen‐Gersdorf, Beyhan Tüysüz(Istanbul University-Cerrahpaşa), Corstiaan C. Breugem(Wilhelmina Children's Hospital), Banu Nur(Istanbul University-Cerrahpaşa), Dulce Papy-García(Centre National de la Recherche Scientifique), Nathalie Séta(Assistance Publique – Hôpitaux de Paris), Christopher T. Gordon(Inserm), Albertien M. van Eerde(University Medical Center Utrecht), Ehsan Ghayoor Karimiani(St George's, University of London), Sandrine Chantepie(Centre National de la Recherche Scientifique), Alexander P.A. Stegmann(Radboud University Nijmegen), Arnaud Bruneel(Inserm), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Caroline Lekszas(University of Würzburg), Ercan Mıhçı(Akdeniz University), Stephan Sonntag(PolyGene), Muriel de La Dure‐Molla(Délégation Paris 5)
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