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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Bibliografiska uppgifter
Huvudupphovsmän: Santos, Maria CLG, Hart, P Suzanne, Ramaswami, Mukundhan, Kanno, Cláudia M, Hart, Thomas C, Line, Sergio RP
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2007
Ämnen:
Research
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1800839/
https://ncbi.nlm.nih.gov/pubmed/17266769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-160X-3-8
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