SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects

Johanne Dubail, Céline Huber, Sandrine Chantepie, Stephan Sonntag, Beyhan Tüysüz, Ercan Mihci, Christopher T. Gordon, Elisabeth Steichen-Gersdorf, Jeanne Amiel, Banu Nur, Irene Stolte-Dijkstra, Albertien M. van Eerde, Koen L. van Gassen, Corstiaan C. Breugem, Alexander Stegmann, Caroline Lekszas, Reza Maroofian, Ehsan Ghayoor Karimiani, Arnaud Bruneel, Nathalie Seta, Arnold Munnich, Dulce Papy-Garcia, Muriel De La Dure-Molla, Valérie Cormier-Daire

Open source

DOI: 10.1038/s41467-018-05191-8
Published: 2018-08-06
Container: Nature Communications
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1038/s41467-018-05191-8,
  title = {SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects},
  author = {Johanne Dubail and Céline Huber and Sandrine Chantepie and Stephan Sonntag and Beyhan Tüysüz and Ercan Mihci and Christopher T. Gordon and Elisabeth Steichen-Gersdorf and Jeanne Amiel and Banu Nur and Irene Stolte-Dijkstra and Albertien M. van Eerde and Koen L. van Gassen and Corstiaan C. Breugem and Alexander Stegmann and Caroline Lekszas and Reza Maroofian and Ehsan Ghayoor Karimiani and Arnaud Bruneel and Nathalie Seta and Arnold Munnich and Dulce Papy-Garcia and Muriel De La Dure-Molla and Valérie Cormier-Daire},
  year = {2018},
  journal = {Nature Communications},
  doi = {10.1038/s41467-018-05191-8},
  url = {https://doi.org/10.1038/s41467-018-05191-8}
}

RIS

TY  - JOUR
TI  - SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects
AU  - Johanne Dubail
AU  - Céline Huber
AU  - Sandrine Chantepie
AU  - Stephan Sonntag
AU  - Beyhan Tüysüz
AU  - Ercan Mihci
AU  - Christopher T. Gordon
AU  - Elisabeth Steichen-Gersdorf
AU  - Jeanne Amiel
AU  - Banu Nur
AU  - Irene Stolte-Dijkstra
AU  - Albertien M. van Eerde
AU  - Koen L. van Gassen
AU  - Corstiaan C. Breugem
AU  - Alexander Stegmann
AU  - Caroline Lekszas
AU  - Reza Maroofian
AU  - Ehsan Ghayoor Karimiani
AU  - Arnaud Bruneel
AU  - Nathalie Seta
AU  - Arnold Munnich
AU  - Dulce Papy-Garcia
AU  - Muriel De La Dure-Molla
AU  - Valérie Cormier-Daire
PY  - 2018
JO  - Nature Communications
DO  - 10.1038/s41467-018-05191-8
UR  - https://doi.org/10.1038/s41467-018-05191-8
ER  -

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., Eerde, A. M. V., Gassen, K. L. V., Breugem, C. C., Stegmann, A., Lekszas, C., Maroofian, R., Karimiani, E. G., Bruneel, A., Seta, N., Munnich, A., Papy-Garcia, D., Dure-Molla, M. D. L., & Cormier-Daire, V. (2018). SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. Nature Communications. https://doi.org/10.1038/s41467-018-05191-8

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crossref · retrieved 2026-09-25T21:08:31.341Z