APA
Dubail J., Huber C., Chantepie S., Sonntag S., Tüysüz B., Mihci E., Gordon C. T., Steichen-Gersdorf E., Amiel J., Nur B., Stolte-Dijkstra I., van Eerde A. M., van Gassen K. L., Breugem C. C., Stegmann A., Lekszas C., Maroofian R., Karimiani E. G., Bruneel A., Seta N., Munnich A., Papy-Garcia D., De La Dure-Molla M. & Cormier-Daire V. (20190107). SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. : Nature communications.
Chicago
Dubail Johanne, Huber Céline, Chantepie Sandrine, Sonntag Stephan, Tüysüz Beyhan, Mihci Ercan, Gordon Christopher T, Steichen-Gersdorf Elisabeth, Amiel Jeanne, Nur Banu, Stolte-Dijkstra Irene, van Eerde Albertien M, van Gassen Koen L, Breugem Corstiaan C, Stegmann Alexander, Lekszas Caroline, Maroofian Reza, Karimiani Ehsan Ghayoor, Bruneel Arnaud, Seta Nathalie, Munnich Arnold, Papy-Garcia Dulce, De La Dure-Molla Muriel and Cormier-Daire Valérie. 20190107. SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. : Nature communications.
Harvard
Dubail J., Huber C., Chantepie S., Sonntag S., Tüysüz B., Mihci E., Gordon C. T., Steichen-Gersdorf E., Amiel J., Nur B., Stolte-Dijkstra I., van Eerde A. M., van Gassen K. L., Breugem C. C., Stegmann A., Lekszas C., Maroofian R., Karimiani E. G., Bruneel A., Seta N., Munnich A., Papy-Garcia D., De La Dure-Molla M. and Cormier-Daire V. (20190107). SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. : Nature communications.
MLA
Dubail Johanne, Huber Céline, Chantepie Sandrine, Sonntag Stephan, Tüysüz Beyhan, Mihci Ercan, Gordon Christopher T, Steichen-Gersdorf Elisabeth, Amiel Jeanne, Nur Banu, Stolte-Dijkstra Irene, van Eerde Albertien M, van Gassen Koen L, Breugem Corstiaan C, Stegmann Alexander, Lekszas Caroline, Maroofian Reza, Karimiani Ehsan Ghayoor, Bruneel Arnaud, Seta Nathalie, Munnich Arnold, Papy-Garcia Dulce, De La Dure-Molla Muriel and Cormier-Daire Valérie. SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. : Nature communications. 20190107.