Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location-Reference-Cited by-同舟云学术

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

Published:2011-03-23 Issue:4 Volume:26 Page:873-880
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Nieminen Pekka,Papagiannoulis-Lascarides Lisa,Waltimo-Siren Janna,Ollila Päivi,Karjalainen Sara,Arte Sirpa,Veerkamp Jaap,Tallon Walton Victoria,Chimenos Küstner Eduard,Siltanen Tarja,Holappa Heidi,Lukinmaa Pirjo-Liisa,Alaluusua Satu

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jbmr.276/fullpdf

Reference22 articles.

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3. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification;Witkop;J Oral Pathol.,1988

4. Hereditary dentin defects;Kim;J Dent Res.,2007

5. Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia;Barron;Orphanet J Rare Dis.,2008

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