Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location

Autor: Janna Waltimo-Sirén, Sirpa Arte, Satu Alaluusua, Eduard Chimenos Küstner, Victoria Tallón Walton, Heidi Holappa, Jaap Veerkamp, Pekka Nieminen, Sára Karjalainen, Lisa Papagiannoulis-Lascarides, Tarja Siltanen, Pirjo-Liisa Lukinmaa, Päivi Ollila

Publikováno v: Nieminen, P, Papagiannoulis-Lascarides, L, Waltimo-Siren, J, Ollila, P, Karjalainen, S, Arte, S, Veerkamp, J, Tallon Walton, V, Chimenos Küstner, E, Siltanen, T, Holappa, H, Lukinmaa, P L & Alaluusua, S 2011, ' Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location ', Journal of Bone and Mineral Research, vol. 26, no. 4, pp. 873-880 . https://doi.org/10.1002/jbmr.276
Journal of Bone and Mineral Research, 26(4), 873-880. Wiley-Blackwell
Journal of Bone and Mineral Research, 26(4), 873-880. American Society for Bone and Mineral Research

We describe results from a mutational analysis of the region of the dentin sialophosphoprotein (DSPP) gene encoding dentin phosphoprotein (DPP) in 12 families with dominantly inherited dentin diseases. In eight families (five mutations in the N-termi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e92dfb999beec60501adfad659759919
https://pubmed.ncbi.nlm.nih.gov/20949630