Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III

Author:

Dong Juan,Gu TingTing,Jeffords Leticia,MacDougall Mary

Funder

National Institute of Dental and Craniofacial Research, National Institute of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference20 articles.

1. Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region;Aplin;J Dent Res,1999

2. An autosomal-dominant form of juvenile periodontitis: Its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc;Boughman;J Craniofac Genet Dev Biol,1986

3. Trinucleotide repeats: Mechanisms and pathophysiology;Cummings;Annu Rev Genomics Hum Genet,2000

4. Gene expression patterns of murine dentin matrix protein 1 (Dmp1) and dentin sialophosphoprotein (DSPP) suggest distinct developmental functions in vivo;D'Souza;J Bone Miner Res,1997

5. Genetic linkage of dentin dysplasia type II to chromosome 4q;Dean;J Craniofac Genet Dev Biol,1997

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