Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

Amelogenesis imperfecta (AI) is a genetically heterogeneous group of diseases that result in defective development of tooth enamel. Mutations in several enamel proteins and proteinases have been associated with AI. The object of this study was to evaluate evidence of etiology for the six major candi...

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Detalles Bibliográficos
Autores principales: Santos, Maria CLG, Hart, P Suzanne, Ramaswami, Mukundhan, Kanno, Cláudia M, Hart, Thomas C, Line, Sergio RP
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1800839/
https://www.ncbi.nlm.nih.gov/pubmed/17266769
http://dx.doi.org/10.1186/1746-160X-3-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1800839/
https://www.ncbi.nlm.nih.gov/pubmed/17266769
http://dx.doi.org/10.1186/1746-160X-3-8

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