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)
FilesNo attached file found for this publication.DetailsAuthorsBastepe, M.AuthorLorenz-Depiereux, B.AuthorBennet-Pages, A.AuthorGhassibé, MichellaUCLouvainAuthorVikkula, MiikkaUCLouvainAuthorJueppner, H.AuthorShow more AffiliationsUCLouvainMD/BICL - Département de biochimie et de biologie cellulaireShow moreCitations APA Chicago FWB 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)