B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation
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Auteurs | Yauy K, Mau-Them FT, Willems M, Coubes C, Blanchet P, Herlin C, Arrada IT, Sanchez E, Faure JM, Le Gac MP, Prodhomme O, Boland A, Meyer V, Riviere JB, Duffourd Y, Deleuze JF, Guignard T, Captier G, Barat-Houari M and Genevieve D |
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Année | 2 018 |
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url DOI | 10.1038/gim.2017.109 |