A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta

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LAUGEL-HAUSHALTER, Virginie, BAR, Severine, SCHAEFER, Elise, STOETZEL, Corinne, GEOFFROY, Véronique, ALEMBIK, Yves, KHAROUF, Naji, HUCKERT, Mathilde, HAMM, Pauline, HEMMERLÉ, Joseph, MANIERE, Marie-Cécile, FRIANT, Sylvie, DOLLFUS, Hélène et BLOCH-ZUPAN, Agnès, sans date. A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta. Frontiers in Genetics. sans date. Vol. 10. DOI 10.3389/fgene.2019.00504. 1. .