An autosomal recessive hypophosphatemic disorder caused by homozygous mutations in dentin matrix protein 1 (DMP1).

Bastepe, M.;Lorenz-Depiereux, B.;Bennet-Pages, A.;Ghassibé, Michella;Jueppner, H.;et.al.
(2006) 28th Annual Meeting of the American-Society-for-Bone-and-Mineral-Research — Location: Philadelphia(Pa) (15.September.2006)

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  • Bastepe, M.
    Author
  • Lorenz-Depiereux, B.
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  • Bennet-Pages, A.
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  • GhassibĂ©, MichellaUCLouvain
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  • Author
  • Jueppner, H.
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Bastepe, M., Lorenz-Depiereux, B., Bennet-Pages, A., Ghassibé, M., Wagenstaller, J., Mueller-Barth, U., Badenhoop, K., Rittmaster, R., Shlossberg, A., Olivares, J., Ramos, F., Vikkula, M., Strom, T., & Jueppner, H. (2006). An autosomal recessive hypophosphatemic disorder caused by homozygous mutations in dentin matrix protein 1 (DMP1). Journal of Bone and Mineral Research, 21, S19. https://hdl.handle.net/2078.5/139567 (Original work published 2006)