A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta by Virginie Laugel-Haushalter, Séverine Bär, Elise Schaefer, Elise Schaefer, Corinne Stoetzel, Véronique Geoffroy, Yves Alembik, Naji Kharouf, Naji Kharouf, Mathilde Huckert, Pauline Hamm, Joseph Hemmerlé, Joseph Hemmerlé, Marie-Cécile Manière, Marie-Cécile Manière, Sylvie Friant, Hélène Dollfus, Hélène Dollfus, Hélène Dollfus, Agnès Bloch-Zupan, Agnès Bloch-Zupan, Agnès Bloch-Zupan, Agnès Bloch-Zupan

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